Endep

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Endep

Property Description
Active Ingredient Amitriptyline Hydrochloride
Form Oral tablets/capsules
Pharmacological Class Tricyclic Antidepressant (TCA)
Common Use Managing depressive symptoms and chronic nerve pain
Origin Synthetic chemical compound

Endep is a prescription-only brand of medicine whose active component is Amitriptyline Hydrochloride. It is a synthetic chemical compound primarily used in the management of mood disorders and certain types of persistent, chronic pain. Endep is supplied as oral tablets, differentiating it as a specific brand formulation of the generic drug amitriptyline.


What Type of Medicine is Endep and How is it Classified?

Endep belongs to the established group of medicines known as Tricyclic Antidepressants (TCAs). This classification reflects its specific chemical structure and how it interacts with neurotransmitter systems in the central nervous system. The medication is typically supplied in an oral form for systemic administration throughout the body.

Amitriptyline is clinically recognized for its role in treating both depression and certain types of chronic pain. This dual recognition helps doctors in situations where a patient requires management for both emotional well-being and persistent physical discomfort.


What is the General Therapeutic Purpose of Endep?

The general therapeutic purpose of Endep is to help manage symptoms associated with major depressive disorder and certain kinds of nerve-related pain (neuropathic pain). It aims to restore the balance of certain natural chemicals in the brain necessary for mental stability and the modulation of pain signals.

Amitriptyline is a TCA used to treat depression. Its versatility means it is often used by doctors for the management of chronic conditions, such as reducing the intensity of pain signals in the nervous system, a therapeutic profile that sets it apart from newer classes of antidepressants.

Regulatory References

  1. US National Library of Medicine (MedlinePlus)

What side effects are possible with Endep?

Possible Side Effects and Safety Information

The official safety characteristics of Endep (Amitriptyline) are documented by regulatory authorities, which categorize possible effects by frequency and the body system they affect. The safety profile is structured to communicate both frequently reported and less common, but clinically significant, adverse reactions.

Adverse Reaction Classification

Side effects are often grouped into System-Organ Classes (SOCs) in official labeling:

  • Nervous and Psychiatric Disorders: Commonly include drowsiness, sedation, dizziness, headache, and tremor. The official documents also cite a risk of suicidal thinking and behavior, particularly in adolescents and young adults (up to age 24) at treatment initiation or following dose adjustment.
  • Cardiovascular Disorders: Documented effects include orthostatic hypotension (a drop in blood pressure upon standing), sinus tachycardia, and disturbances in heart rhythm. Serious adverse reactions such as myocardial infarction and stroke are listed in regulatory sources.
  • Gastrointestinal Disorders: Very common effects typically involve dry mouth and constipation. Other effects include nausea and vomiting.
  • Other Common Effects: Blurred vision, urinary retention, and weight gain are commonly noted in prescribing information.

Population and Duration-Related Safety

Safety constraints exist for specific patient groups. Older adults are noted to have increased susceptibility to orthostatic hypotension, which may lead to falls, and confusion. Careful consideration is required for those with known hepatic impairment. The medicine is strictly restricted for use during the acute recovery phase following myocardial infarction and is contraindicated for use with Monoamine Oxidase Inhibitors (MAOIs). After prolonged administration, regulatory documents state that abrupt cessation may be associated with withdrawal symptoms such as headache, irritability, and malaise.

Overdose and Emergency Response

Overdose and When to Seek Help

Overdose with Endep (amitriptyline) is a serious medical emergency requiring immediate attention, even if no symptoms are present. Ingestion of 750 mg or more in an adult can lead to severe toxicity. Overdose effects typically develop within 30 minutes to 6 hours after ingestion.

Immediate medical help must be sought if an overdose is suspected, or if a person has collapsed, experienced a seizure, has trouble breathing, or cannot be awakened. Toxicity is increased when Endep is taken with alcohol or other substances.

Documented Overdose Manifestations

System Symptoms
Central Nervous System (CNS) Coma, seizures, agitation, hallucinations, confusion, muscle rigidity, tremor.
Cardiovascular Irregular heart rhythm (arrhythmias), rapid heart rate (tachycardia), severe low blood pressure (hypotension), QRS/QT prolongation, cardiac arrest.
Anticholinergic Blurred vision, dry mouth, dilated pupils, urinary retention, severe constipation.
Respiratory Slowed or labored breathing, respiratory arrest.

Emergency Response

Treatment is symptomatic and supportive, requiring admission to a hospital or intensive care unit. Continuous ECG monitoring of heart function is necessary for several days. Vomiting should not be induced. Due to the high risk of rapid, severe cardiovascular and CNS complications, immediate medical assessment is mandatory for all suspected overdoses.

Therapeutic Uses of Endep

Endep (Amitriptyline) may be part of symptomatic management across two distinct therapeutic domains: mood support and chronic pain management.

Endep is commonly used across conditions presenting with systemic or localized discomfort, applying to depressive illnesses like Major Depressive Disorder. It is relevant for easing symptom clusters that may become intense or disruptive, such as persistent low mood and emotional distress. This supportive therapeutic benefit assists with maintaining functional stability, contributing to improved comfort during periods of heightened symptoms.

The medication is also commonly used when short-term symptomatic assistance is needed, particularly for chronic neuropathic pain and other persistent pain syndromes. It addresses symptoms related to increased neurological activity, such as burning and shooting pains, and is applied across domains where additional symptomatic support is needed for recurrent neurological pain events like migraine headaches. The core therapeutic uses generally include management of symptoms related to systemic imbalance in Major Depressive Disorder, addressing symptoms related to physical discomfort in chronic neuropathic pain, and supportive relief for conditions involving episodic or fluctuating manifestations. As summarized: “Provides support that helps ease the overall symptom burden.”


Quick Fact: Symptomatic Relief for Physical Discomfort Endep is commonly used to help manage symptoms related to physical discomfort and increased neurological activity, assisting with maintaining functional stability.

Regulatory References

  1. NIH MedlinePlus overview of Amitriptyline

Eligibility and Restrictions for Use

Who Can and Cannot Use Endep? (Official Regulatory Information)

Endep (Amitriptyline) is officially approved for use in adult patients. Eligibility is strictly governed by national regulatory guidelines that define absolute contraindications and conditional-use populations.

Eligibility Status Patient Population / Condition
Contraindicated (Must Not Use) Acute recovery phase following Myocardial Infarction (MI).
Known hypersensitivity to Amitriptyline or concurrent use of Monoamine Oxidase Inhibitors (MAOIs).
Severe heart problems, including heart block, certain arrhythmias, or severe liver disease.
Restricted Use/Caution History of seizures, urinary retention, or angle-closure glaucoma.
Geriatric patients (65+ years) due to the need for cautious selection and adjustment.
Use Not Recommended Children and adolescents under 18 years (or under 12 years in some regions), as safety and efficacy are not established.

Pregnancy and Lactation: The official status for use during pregnancy is conditional; it is recommended only if the potential therapeutic benefit to the mother is determined to justify the potential risk to the fetus. The compound is secreted into breast milk, and use while nursing requires a careful weighing of the benefits versus potential infant effects.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Endep (Amitriptyline) has officially documented interaction patterns based on its classification as a Tricyclic Antidepressant (TCA). The regulatory profile establishes specific prohibited combinations and risk factors associated with metabolism and pharmacodynamic effects.

Official Interaction Statements

Co-administration with Monoamine Oxidase Inhibitors (MAOIs) is formally contraindicated due to the high risk of a severe, potentially fatal Serotonin Syndrome. To prevent this acute pharmacodynamic interaction, a mandatory 14-day separation period must elapse after discontinuing an MAOI before initiating Amitriptyline therapy.

Pharmacokinetic and Pharmacodynamic Risks

  • Metabolic Clearance Inhibition: Inhibition of CYP2D6 by co-administered medicinal products, such as Fluoxetine or Cimetidine, results in increased plasma concentrations of Amitriptyline. This is an official exposure-altering effect.
  • Additive Pharmacodynamic Effects: Co-administration with CNS Depressants (including alcohol) or other Serotonergic Drugs amplifies the central nervous system effects. The label states that Amitriptyline may enhance the response to alcohol and other sedatives.
  • Cardiac Conduction Risk: Combining Amitriptyline with other QTc-prolonging agents (e.g., Cisapride, Pimozide, Thioridazine) is strictly prohibited due to the heightened risk of ventricular arrhythmias.

These official interaction statements govern the necessary time constraints and exposure monitoring requirements for co-administering the drug with other substances.

Mechanism of Action

Mechanism of Action: Amitriptyline

The fundamental mechanism of the active compound, amitriptyline, involves the inhibition of the Norepinephrine Transporter ( NET) and the Serotonin Transporter ( SERT), which prevents the reabsorption of these neurotransmitters. This action increases the concentration of NE and 5-HT in the synapse, enhancing the activity of the descending inhibitory pathways in the spinal cord and contributing to the modulation of central monoaminergic signaling.

Simultaneously, the compound acts directly on neuronal membranes by blocking Voltage-Gated Sodium Channels ( VGSCs). This stabilizes the electrical potential of the nerve cell, limiting the spontaneous electrical discharge of impulses and contributing to a reduction in the transmission of excessive nerve signals. The drug also exhibits non-selective antagonism at Histamine H1 and Muscarinic M1 receptors, which alters CNS arousal levels and modulates autonomic signaling, contributing to the overall pharmacological effect profile.

Dosage and Administration Information

How Endep (Amitriptyline) is Used: Official Administration Guidelines

Endep, a brand formulation of amitriptyline hydrochloride, is intended solely for oral administration as tablets. The usage protocol is characterized by specific starting doses, gradual adjustment, and population-specific modifications.

Official Dosing and Frequency

The total daily dose of Endep is typically administered once daily, preferably taken at bedtime. Alternatively, the dose may be administered in divided doses throughout the day. It can be taken with or without food. The dosage depends on the condition being addressed:

Condition Typical Starting Dose Maximum Daily Dose (Outpatient)
Depression 75 mg daily 150 mg/day
Neuropathic Pain 10 mg to 25 mg daily 75 mg/day (often lower for pain)

Procedural Administration Steps

The initiation of use requires a gradual dosage increase, known as titration. The dose is typically adjusted in small increments, often 10 mg to 25 mg, over several days until the maintenance level is reached. A therapeutic effect for depression may take up to 30 days to fully develop.

Population-Specific Use

Dose reductions are required for specific populations. Older adults (geriatric patients) require lower initial doses, often starting at 30 mg to 75 mg daily or less, and doses above 75 mg are advised with caution. A dose reduction of approximately 50% of the recommended starting dose should be considered for patients with hepatic impairment. Upon cessation of use, the medicine must be gradually reduced over a period of several weeks to properly conclude the course of treatment.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Endep (Amitriptyline)

This section summarizes the type of research that has explored Endep (amitriptyline), describing the focus of the studies, the outcomes measured, and the known limitations in the existing evidence, without offering clinical recommendations or advice.


Evidence for Use in Major Depressive Disorder (MDD)

The research base for Endep has explored its use in major depressive disorder is structured around many older Randomized Controlled Trials (RCTs) conducted over several decades, which were then summarized in Systematic Reviews and Meta-analyses. Research focused on comparing Endep with an inactive placebo or with other compounds studied for similar conditions. Researchers examined patient-reported outcomes describing discomfort and changes in the intensity of depressive symptoms.

Scientific reviews consistently point out that the evidence quality varies across studies, citing concerns like modest methodological reporting in older trials. This means that while many studies exist, the certainty of the findings in current reviews may be assessed as Low to Moderate due to these limitations.

Evidence for Chronic Neuropathic Pain Conditions

The use of Endep has also been evaluated in conditions characterized by fluctuating or episodic manifestations, including specific research on pain associated with nerve-related conditions (neuropathic pain). Research examined trials assessing short-term symptom patterns and comparing Endep to an inactive substance or to compounds studied for pain. Findings describe patterns observed in the studies related to the proportion of participants who reported different measurements on pain scales and on scales assessing associated factors like sleep.

Scientific reviews typically suggest that the certainty remains low for many of the chronic pain indications. Key limitations include the fact that follow-up durations were limited, often running for only 4 to 12 weeks, which provides limited insight into long-term pain management.

What Research Remains Incomplete or Uncertain

Data for certain groups, such as those with specific comorbidities or in certain age groups, remain insufficient. Furthermore, the small sample sizes and methodological flaws in many of the older trials mean that the findings may be less consistent than those from modern, large-scale studies. Long-term effects have not been well characterized on sustained daily functioning and activity level. Evidence related to newer treatment classes is also an area where research is ongoing.

Key Studies & References

  1. Amitriptyline: MedlinePlus Drug Information

Frequently Asked Questions (FAQ)

Common questions about Endep (FAQ)

Q: How quickly can a person expect to feel the effects of Endep?

According to official product information, the full therapeutic benefit for depression may take up to 30 days to develop. However, some people may notice earlier changes, such as improved sleep, within the first week of use.

For chronic nerve-related pain, it often requires a period of four to six weeks before the full benefit is observed.

Q: Does Endep have a different purpose when prescribed at very low doses?

Regulatory documents indicate that Endep is prescribed at higher doses for depression and at much lower initial doses for certain chronic nerve pain conditions.

This difference in dosing reflects its use in modulating nerve signals for pain management, which is a key therapeutic purpose separate from its antidepressant role.

Q: What happens if I stop taking Endep suddenly?

Stopping Endep suddenly is strongly discouraged and not recommended in official guidelines because the body adapts to the medication. Abrupt cessation can be associated with withdrawal symptoms such as headache, nausea, and general malaise or irritability.

Official guidelines state that a healthcare provider must manage a gradual reduction in dose to safely conclude treatment.

Q: What are the long-term safety concerns or effects of taking Endep?

Regulatory safety information notes potential concerns associated with prolonged use of tricyclic antidepressants. These include a need for close monitoring regarding the risk of heart rhythm disturbances (such as arrhythmias).

Additionally, documented but rare concerns include a risk of bone fracture and potential effects on liver function, and monitoring for these effects may be required.

Q: How does Endep interact with common over-the-counter pain relievers?

Official drug labels warn against combining Endep with substances classified as CNS depressants to avoid excessive sedation.

While common over-the-counter pain relievers like ibuprofen or acetaminophen are not typically contraindicated, any daily or near-daily use of relief medication should be discussed with a healthcare provider.

Q: Is it true that Endep can cause a 'hangover' or groggy feeling in the morning?

Yes, it is common for Endep to cause effects like drowsiness, sedation, and dizziness because it is a sedating medication. Due to the drug's nature, these effects can persist and result in a feeling of being groggy or unrested when waking up the following morning.

This is why the medication is often recommended to be taken at bedtime.

Q: Can Endep cause confusion or difficulty with memory, especially in older adults?

Official prescribing information notes that Endep can cause both confusion and memory disturbances. This risk is considered particularly relevant for older adults, who may be more susceptible to these effects.

Due to this susceptibility, official guidelines often recommend lower starting doses for older adults.

Q: Is it safe to consume alcohol while taking Endep?

Regulatory information warns that Endep may enhance the body's response to alcohol. Since alcohol is a CNS depressant, combining it with Endep amplifies the effects on the central nervous system, increasing the risk of over-sedation and potentially dangerous consequences.

The interaction between Endep and alcohol should be discussed with the prescribing healthcare provider.

Q: Why does Endep sometimes cause a dry mouth?

The reason for dry mouth is related to Endep's anticholinergic properties.

This action involves blocking nerve signals that typically stimulate saliva production in the mouth, which results in a reduction of saliva flow. Dry mouth is listed as a very common side effect in official documents.

Q: Are there specific food or drink restrictions while taking Endep?

Endep can be taken with or without food, as directed by a healthcare provider. The primary drink restriction noted in official documents is alcohol due to the enhanced CNS depressive effects.

Additionally, caution is generally advised when consuming excessive amounts of caffeine, as both substances can affect heart rate.

Q: What are the signs of a serious or dangerous reaction to Endep?

Official consumer safety information lists several serious reactions that require immediate medical attention. These include signs of Serotonin Syndrome (such as agitation or rigid muscles), indications of heart problems (like a sudden fast heartbeat or fainting), and unexplained bleeding or bruising.

Furthermore, an increased risk of suicidal thoughts or changes in behavior is listed as a serious warning, particularly at the start of treatment.

Q: Is Endep safe to take during pregnancy or while breastfeeding?

For pregnancy, official documents indicate that use is conditional; it is recommended only if the potential therapeutic benefit to the mother is determined to justify the potential risk to the developing fetus.

For breastfeeding, the compound is known to pass into breast milk, and use requires a careful medical weighing of the benefits of therapy against any potential infant effects.

Q: How long does it typically take to gradually stop taking Endep?

The process for stopping Endep requires a gradual reduction in dosage, typically spanning a period of several weeks. This process is not instant; the reduction process should be carefully managed by a healthcare provider to prevent the onset of withdrawal symptoms.

The exact duration of the tapering schedule will depend on the dose being taken and the overall length of treatment.

Q: What is the significance of the anticholinergic side effects of Endep?

The term anticholinergic describes a key property of Endep that affects nerve signaling. The significance is that this action is responsible for many common side effects, including dry mouth, blurred vision, difficulty urinating, and confusion.

The intensity of this anticholinergic action is a distinguishing feature of Endep among other similar medications.

Q: Is there a maximum time a person can safely take Endep?

Official regulatory documents do not specify a single maximum time limit for taking Endep. Instead, the guidance emphasizes that once a person achieves improvement, the dose should be reduced to the lowest effective amount necessary to maintain that relief.

For certain conditions like depression, maintenance therapy is often continued for at least three months or longer to help prevent a relapse.

Q: What kind of studies support the use of Endep for fibromyalgia?

Research evidence focuses on the use of Endep for chronic neuropathic pain conditions generally. Although the official label does not specifically name fibromyalgia, studies examining this broader category of nerve-related pain indicate that Endep has been shown to reduce symptoms.

These trials are often of limited duration, typically lasting only a few months.

Q: Is the drowsiness from Endep useful for people who have trouble sleeping due to pain?

Yes, the sedating effect of Endep is often leveraged therapeutically. Due to its pronounced drowsiness, the medicine is typically administered as a single dose right before bedtime.

This dosing strategy is utilized to both minimize daytime sedation and potentially assist patients whose persistent pain makes it difficult for them to fall or stay asleep.

Q: Is it safe to drive or operate machinery while taking Endep?

Due to the risk of common side effects such as drowsiness, sedation, dizziness, and blurred vision, official documents explicitly warn against driving a vehicle or operating hazardous machinery.

The official warning advises patients to wait until they are reasonably certain that the medication does not adversely affect their ability to perform these tasks.

Q: Can Endep cause changes in appetite?

Yes, official side effect listings indicate that Endep can cause changes in appetite. Regulatory documents list both decreased appetite and, more commonly, increased appetite.

This change in appetite often contributes to the reported side effect of weight gain.

Q: Why is Endep sometimes given as a single dose at bedtime?

The single dose is preferably taken at bedtime to take advantage of the medicine's pronounced sedative properties.

This approach helps to minimize the impact of common side effects like drowsiness and dizziness during the daytime, making the drug easier to tolerate for many patients.

Q: What are the differences in how Endep is processed by the body in older vs younger adults?

Regulatory information notes differences in how the body processes Endep based on age. Older adults and those with liver issues may experience a longer half-life, meaning the drug stays in the body longer before it is eliminated.

This difference in processing is why official guidelines recommend that healthcare providers consider lower starting doses and monitor older patients closely for signs of increased side effects.

Q: Is Endep the same as other TCAs like Elavil or Tryptizol?

Yes, Endep, Elavil, and Tryptizol are all different brand names used in various countries for the same single active chemical compound: amitriptyline hydrochloride.

All these formulations belong to the class of tricyclic antidepressants.

Q: Is Endep considered addictive or habit-forming?

No, authoritative guidance indicates that Endep is not considered addictive or habit-forming in the way that controlled substances are classified. However, the body does adapt to the medication over time, which is why abruptly stopping treatment can cause uncomfortable symptoms of physical withdrawal.

Q: Are there different types of side effects for Endep when used for depression versus for chronic pain?

Regulatory documents list the possible side effects generally for the medication, without differentiating between the depression and chronic pain indications. However, because the dose used for chronic pain management is often substantially lower than the dose used for depression, the incidence or severity of common side effects like sedation, dry mouth, and confusion may be less pronounced.

Q: What common supplements or herbal remedies interact with Endep?

Official drug labels and warnings advise caution with many complementary medicines. The most commonly cited herbal remedy that interacts with Endep is St John's wort, which can increase the risk of serious side effects.

Official warnings advise discussing the use of any herbal or unapproved complementary medicines with a healthcare provider.

Q: Can Endep affect sleep quality in ways other than making a person sleepy?

Yes, while Endep is known for its sedating properties, the official side effect profile also lists uncommon adverse reactions related to sleep. These include reports of insomnia and nightmares, which indicate that the drug can disrupt the normal architecture and quality of sleep in some individuals.

Q: How long does Endep stay in the body after the last dose?

The active component of Endep has an elimination half-life typically ranging from 12 to 36 hours. However, the medication is metabolized into an active chemical called nortriptyline, which has an even longer half-life.

Because of this process, the medicine's effects and presence in the body can persist for several days after the final dose is taken.

Q: Is Endep a medication that needs to be taken at the same time every day?

While the official guideline specifies the dose is typically administered once daily (often at bedtime), taking the medication at the same general time each day is standard practice.

This consistency helps to maintain steady levels of the drug in the body, which is important for ensuring the therapeutic effect is sustained.

Q: Is it possible to develop a tolerance to the side effects of Endep over time?

Yes, it is a common observation that the initial intensity of certain side effects, particularly drowsiness, dry mouth, or lightheadedness, typically lessens or improves within the first few weeks of starting the medicine.

This natural adjustment period is often described by patients as developing a tolerance to those particular effects.

Q: How does Endep affect or change a person's sexual function or drive?

The side effect profile for Endep includes potential effects on sexual function. Regulatory documents list reports of erectile dysfunction in men and a generalized decrease in sex drive (libido) for both men and women.

These effects are considered possible but not guaranteed for all patients.

Q: Does Endep have any known interactions with recreational drugs?

Official drug interaction warnings explicitly advise against combining Endep with other substances that affect the central nervous system, including certain recreational drugs. Because Endep is an additive CNS depressant, combining it with other sedating or mood-altering substances can amplify the effects, significantly increasing the risks of over-sedation and dangerous consequences.

Q: Why do people sometimes experience strange or vivid dreams on Endep?

Official regulatory documents list nightmares as an uncommon but documented adverse reaction to Endep.

Although the specific cause is not always stated, this side effect indicates that the medicine can alter the body's patterns of sleep and dreaming.

Q: Can Endep increase sensitivity to sunlight?

Yes, the official side effect profile lists a photosensitivity reaction as a rare adverse effect. This means Endep can potentially increase the sensitivity of the skin to sun exposure.

Because of this, protective measures against sun exposure, such as wearing sunscreen, are often recommended when taking this medicine.

Q: Does Endep affect blood sugar levels for people with or without diabetes?

Yes, official side effect listings indicate that Endep can impact blood sugar levels. Documented effects include both the elevation and lowering of blood sugar.

Monitoring blood sugar levels may be required for patients who have diabetes or who are otherwise at risk.

Q: Is it true that Endep can affect fertility in men or women?

Based on current regulatory and authoritative guidance, there is no evidence indicating that Endep affects fertility in either men or women. While information is provided regarding use during pregnancy and breastfeeding, fertility is not listed as a known concern.

Q: Is Endep's mechanism of action fully understood for non-depressive uses like pain?

While the drug's action on neurotransmitters like norepinephrine and serotonin is known, the full mechanism for all uses, particularly for pain relief, is not yet completely elucidated.

Current understanding suggests the pain-relieving effects are mediated by its influence on these chemicals, which are critical components of the body's descending inhibitory pain pathways.

How should Endep be stored and disposed of?

How to Store and Dispose of Endep?

Endep (amitriptyline hydrochloride) tablets must be stored according to official regulatory requirements to maintain product stability and safety.


Storage Requirements

Condition Regulatory Requirement
Temperature Store at Controlled Room Temperature, 20 C to 25 C (68 F to 77 F). Do not freeze or expose to excessive heat.
Container Keep in the container it came in, tightly closed. Dispense in a tight, light-resistant container.
Protection Protect from excessive light and moisture.
Child Safety Must be kept out of the reach of children.

️ Disposal Instructions

Unused or expired Endep must be disposed of according to local regulations. This often involves using official drug take-back programs or designated disposal facilities rather than discarding in household trash or flushing down a toilet.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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