Azo-Ciproflox

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Azo-Ciproflox

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Medically reviewed

Marina Burgos

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 Azo-Ciproflox

Defining Azo-Ciproflox: A Combination Anti-Infective

Property Description
Active Ingredients Ciprofloxacin, Phenazopyridine
Form Oral Solid Dosage Form (Tablet)
Pharmacological Class Quinolone Antimicrobial + Urinary Tract Analgesic
Origin Synthetic Compounds
Type Fixed-Dose Combination Product

Azo-Ciproflox is a synthetic fixed-dose combination product containing two distinct active ingredients: the antimicrobial agent Ciprofloxacin and the urinary analgesic Phenazopyridine. This means the medication belongs to a dual pharmacological class, specifically a quinolone antimicrobial used in conjunction with a substance for pain relief, a combination approach clinically recognized for managing infectious processes that cause significant local discomfort. Its unique identity lies in the simultaneous administration of these two distinct, chemically synthesized components.


Composition and Form: Dual-Action Oral Therapy

This preparation is delivered as an oral solid dosage form, typically a tablet, which integrates both active compounds into a single unit. The formulation ensures that the Ciprofloxacin component, which performs the bactericidal action, is combined with the Phenazopyridine component, which provides local comfort. The oral route of administration simplifies the therapeutic strategy by ensuring the patient receives both the necessary anti-infective and the symptom-alleviating components simultaneously, streamlining the treatment approach compared to administering two separate medications.


What is the General Purpose of Combining Ciprofloxacin and Phenazopyridine?

The general purpose of this combination is to provide a comprehensive dual-action approach for managing conditions involving both microbial presence and significant local discomfort. The Ciprofloxacin component, a synthetic broad-spectrum fluoroquinolone drug, is included to provide the essential function of eliminating the root cause of the infection.

Conversely, the addition of the Phenazopyridine component is purposed solely to offer immediate symptomatic relief by exerting a local anesthetic effect on the urinary tract mucosa. This pairing allows for the effective elimination of the pathogen while simultaneously addressing the patient's immediate and tangible need for comfort during the course of anti-infective treatment.

Regulatory References

  1. WHO Essential Medicines List (eEML)
  2. MedlinePlus Drug Information for Phenazopyridine

What side effects are possible with Azo-Ciproflox?

Possible side effects and safety information

This section describes the safety characteristics and officially documented adverse reactions of Azo-Ciproflox, derived from government regulatory documents. The profile integrates the risks associated with the quinolone antimicrobial, Ciprofloxacin, and the urinary analgesic, Phenazopyridine.


Serious Adverse Reactions and Warnings

The quinolone component is associated with official regulatory warnings regarding disabling and potentially irreversible serious adverse reactions. These include effects on the tendons (e.g., tendinitis and tendon rupture), peripheral nerves (peripheral neuropathy), and the central nervous system (CNS effects). Other serious documented reactions include the risk of Aortic Aneurysm and Dissection, QT interval prolongation, and the exacerbation of muscle weakness in patients with Myasthenia Gravis.


Common Adverse Reactions and Organ Systems

Adverse events classified as common (reported at an incidence ge 1% in regulatory clinical data) typically involve the Gastrointestinal System, including nausea, diarrhea, and vomiting. Other frequently documented reactions include rash, headache, and abnormal liver function tests. The analgesic component may cause headache, rash, and occasional gastrointestinal disturbance.


Safety Restrictions and Special Populations

Phenazopyridine is contraindicated in individuals with severe renal or hepatic impairment due to the risk of drug accumulation. The regulatory label for the analgesic component stipulates that its use with an antibacterial agent should not exceed two days. The quinolone component is reserved for uncomplicated cystitis only when alternative treatments are unavailable. In older adults, there is an increased risk of tendon disorders, especially when corticosteroids are used concurrently. Phenazopyridine also imparts a reddish-orange discoloration to urine and other body fluids, a safety characteristic noted in official labeling.

Overdose and Emergency Response

Overdose Manifestations and Emergency Action

Official regulatory documents define the Azo-Ciproflox overdose profile based on the combined toxicities of its two components, Ciprofloxacin and Phenazopyridine. An overdose of the Ciprofloxacin component may be identified by Central Nervous System (CNS) manifestations, including confusion, tremor, hallucinations, and seizures (convulsive status epilepticus). Renal toxicity is also a documented risk, specifically the formation of crystalluria which may lead to acute renal failure.

The Phenazopyridine component is formally associated with the severe hematological risks of methemoglobinemia and hemolytic anemia. Population-specific considerations note increased risks for patients with existing CNS disorders or G6PD deficiency.

When to Seek Immediate Medical Help

Due to these severe and potentially life-threatening outcomes, regulatory guidance mandates that users seek immediate medical attention and contact a poison control center or emergency services in the event of suspected overdose. Management protocols described in official labeling include immediate measures such as gastric evacuation and activated charcoal administration to reduce absorption, alongside symptomatic and supportive treatment. ECG monitoring and intensive clinical observation are required, and Methylene blue is cited as the specific intervention for methemoglobinemia.

Therapeutic Uses of Azo-Ciproflox

What Azo-Ciproflox Treats: Main Uses and Benefits

The combination medication Azo-Ciproflox is generally applied in clinical settings that involve acute or disruptive symptom patterns associated with lower urinary tract infections (UTIs). It is a dual-action therapy considered relevant for adults with bacterial cystitis where immediate and pronounced discomfort is present.

This therapy is commonly used in conditions characterized by periods of heightened symptoms of lower UTIs. It utilizes the anti-infective component to address the bacteria contributing to the infection, offering the core therapeutic benefit of pathogen management and assisting with the overall management of the underlying condition. The formulation is applied to ease symptom clusters that may become intense or disruptive, such as acute dysuria (painful urination), burning, and urinary urgency/frequency.

The analgesic component is applied to ease these symptoms related to inflammatory or irritative states in the urinary tract. This approach provides support that helps ease the overall symptom burden and provides supportive relief when symptoms interfere with routine activities.

“The combination is used to offer symptomatic relief that may help support the patient during episodes of heightened discomfort while the anti-infective treatment is applied.”

The conditions for which this dual approach is commonly used include acute cystitis and other lower urinary tract infections that present with significant pain.


Quick Fact: Relief for Acute Dysuria
This combination is most relevant when symptoms related to physical discomfort—specifically the pain and burning sensation during urination—are interfering with daily functioning.

Regulatory References

  1. NIH MedlinePlus overview of Phenazopyridine use

Eligibility and Restrictions for Use

Who Can and Cannot Use Azo-Ciproflox?

The eligibility for Azo-Ciproflox is determined by the official restrictions of its two components: Ciprofloxacin (a fluoroquinolone antimicrobial) and Phenazopyridine (a urinary analgesic). This medication is generally intended for use by adults who do not have documented contraindications.


Absolute Contraindications

Use is prohibited by regulatory documents for several groups, primarily due to the Ciprofloxacin component. The medicine is contraindicated in patients with a history of allergic reactions to any fluoroquinolone or to Phenazopyridine itself, a history of tendon rupture associated with fluoroquinolone use, or those diagnosed with Myasthenia Gravis. The Phenazopyridine component makes the combination contraindicated in patients with severe renal or hepatic insufficiency.


Age and Physiological Restrictions

This medication is contraindicated in children and adolescents under 18 years of age due to the risk of joint damage associated with fluoroquinolones. Use is not recommended during pregnancy or lactation (breastfeeding).

Conditional Use

Use requires caution in patients with certain conditions, including known QT interval prolongation, epilepsy or a history of seizures, and in older adults due to an increased risk of severe tendon issues.

What should I know about interactions with other medicines?

The interaction profile of Azo-Ciproflox is primarily determined by its Ciprofloxacin component. Co-administration with Tizanidine is contraindicated due to Ciprofloxacin's inhibitory effect on Tizanidine metabolism, which causes Tizanidine concentrations to increase significantly. Ciprofloxacin is a known inhibitor of the CYP1A2 enzyme, leading to elevated plasma levels of other medicines metabolized by this pathway, such as Theophylline, Caffeine, and Clozapine.

The concurrent use of Ciprofloxacin with products containing multivalent cations severely reduces Ciprofloxacin bioavailability. These include Antacids (aluminum or magnesium-based), and Iron or Zinc supplements. To avoid this pharmacokinetic reduction, a mandatory separation time is required: these supplements must be administered at least 2 hours before or 6 hours after the Ciprofloxacin dose. Ingestion with dairy products or calcium-fortified juices alone is also noted to decrease absorption.

Pharmacodynamic interactions include the potential enhancement of the anticoagulant effect of Warfarin. Co-administration with other QT-prolonging drugs may pose an additive risk to the heart's electrical system. Furthermore, drugs like Probenecid reduce Ciprofloxacin's renal clearance, resulting in increased systemic drug concentrations. For the Phenazopyridine component, there is a risk of accumulation noted in patients with impaired renal function.

Mechanism of Action

The dual mechanistic profile of Azo-Ciproflox is defined by two independent actions: one focused on microbial cytotoxicity and the other on peripheral neural signaling.


Disruption of Bacterial Genetic Machinery

The antimicrobial component, Ciprofloxacin, executes its mechanism by targeting the essential bacterial enzymes, DNA Gyrase and Topoisomerase IV. Ciprofloxacin stabilizes the complex formed between the enzyme and the DNA strand, preventing the crucial re-ligation step. This inhibition results in the accumulation of irreversible double-stranded DNA breaks that halt prokaryotic replication. This targeted disruption of the microbial genetic machinery is the core mechanism that results in microbial cell death.


Localized Modulation of Sensory Nociception

The second component, Phenazopyridine, provides a strictly topical anesthetic action upon its excretion and concentration in the urine. It interacts directly with afferent sensory nerve endings within the lower urinary tract mucosa, stabilizing the neural membrane and suppressing the generation and conduction of nerve impulses. This localized mechanism results in the attenuation of afferent sensory signaling and reduces the magnitude of nerve transmission originating from the tissue.

Dosage and Administration Information

The administration of Azo-Ciproflox is defined by official protocols that govern the timing and duration of this fixed-dose oral combination. The product is administered twice daily (every 12 hours). For acute uncomplicated cystitis, the Ciprofloxacin component typically aligns with a 250 mg dose per intake. The tablet is required to be taken with or immediately following food or a snack to mitigate potential gastrointestinal discomfort and must be swallowed with adequate water.

A critical usage constraint dictates that the combination tablet, due to the presence of Phenazopyridine, must not exceed 2 days (four doses). After this period, the patient is officially required to discontinue the fixed-dose product and continue the Ciprofloxacin component alone to complete the full mandated antimicrobial course, which is commonly 3 days for this indication.

A key restriction in administration involves separating the tablet intake from products containing multivalent cations (such as magnesium or aluminum antacids or mineral supplements) by several hours. This procedural step is necessary to prevent diminished absorption of the Ciprofloxacin component. Furthermore, dose modification is officially required for patients with impaired renal function, and the Phenazopyridine component should be avoided in cases of renal insufficiency.

Recent Clinical Evidence

Azo-Ciproflox: Recent Clinical Evidence

Evidence Base for Acute Bacterial Cystitis and Symptoms

The research base for this combination therapy was studied for conditions associated with acute or disruptive episodes of lower urinary tract infection (UTI), specifically acute bacterial cystitis. The evidence primarily data show patterns related to Randomized Controlled Trials (RCTs) that have evaluated the anti-infective component (Ciprofloxacin) in research contexts involving lower urinary tract infections (UTIs), often comparing it to other antimicrobial agents. Systematic reviews, which synthesize data from multiple RCTs, also contribute to the broader evidence landscape.

These studies research examined two main categories of outcomes: Microbial Outcomes (linked to measuring changes in the uropathogen population) and Clinical Outcomes (applied in studies examining patient-reported experiences). The main populations was studied for this evidence are adult women with uncomplicated cystitis.

Research on Drug Behavior: Pharmacokinetic Studies

The unique combination of the two medications in a single tablet was studied for research exploring how the body processes them together. This area was evaluated in pharmacokinetic (PK) studies designed as randomized, crossover trials. The studies monitored Systemic Exposure Parameters such as the highest drug concentration achieved ( Cmax) and total drug exposure (AUC). The findings contribute to understanding the bioavailability characteristics of the anti-infective agent within the combined formulation.

Long-Term Outcomes, Special Populations, and Uncertainty

The key clinical studies utilize follow-up periods that vary widely, ranging from short-term assessments (days) to intermediate-term observations (four to eight weeks) was studied for assessing the potential return of infection. While these longer follow-up periods contribute to understanding symptom patterns over time, long-term effects are not fully established or consistently reported across all research.

Research on the anti-infective component was evaluated in adult women with uncomplicated UTIs. However, the specialized PK studies were often conducted in healthy adult volunteers, limiting direct insight into absorption characteristics in patients with active infection. Evidence is limited regarding the clinical impact of the fixed-dose combination product compared directly to administering the two medications separately. The research evidence highlights what is known — and what is still uncertain.

Key Studies & References

  1. Phenazopyridine: MedlinePlus Drug Information

Frequently Asked Questions (FAQ)

Common questions about Azo-Ciproflox (FAQ)


Q: Does Azo-Ciproflox treat the infection itself?

A: Azo-Ciproflox is a combination product with dual functions. The Ciprofloxacin component is the antimicrobial agent responsible for killing the bacteria and addressing the infection. However, the Phenazopyridine component is included only to provide temporary, symptomatic relief and does not contribute to curing the infection.

Q: What is the difference between Azo-Ciproflox and just Ciprofloxacin?

A: The key difference is that Azo-Ciproflox is a fixed-dose combination product containing two active ingredients. It includes the anti-infective Ciprofloxacin plus the urinary tract analgesic Phenazopyridine in a single tablet. Ciprofloxacin alone contains only the antibiotic agent.

Q: Can Azo-Ciproflox be used for a kidney infection?

A: Official information indicates that the Ciprofloxacin component is used for certain formulations to treat pyelonephritis (kidney infection). However, the specific combination product is typically reserved for uncomplicated cystitis, and the Phenazopyridine component is often contraindicated in cases of pyelonephritis of pregnancy.

Q: Is it common to feel dizzy after taking Azo-Ciproflox?

A: Dizziness is a possible adverse reaction documented in official labeling for the Ciprofloxacin component, often categorized under Central Nervous System (CNS) effects. It is also listed as a less frequent or incidence-unknown side effect for Phenazopyridine. Concerns about unexpected or severe dizziness should be discussed with a healthcare professional.

Q: Is Azo-Ciproflox safe to take with common pain relievers like Tylenol or Advil?

A: The Phenazopyridine component is generally not known to interact directly with common pain relievers such as acetaminophen (Tylenol) or ibuprofen (Advil). Official labeling does not typically list these common pain relievers as restricted, though they are not formally studied in combination. The product labeling for the antimicrobial component lists other specific drug interactions to avoid.

Q: Can older adults safely use Azo-Ciproflox?

A: Official labeling notes that older patients (usually over 60) have an increased risk of specific serious adverse reactions related to the Ciprofloxacin component. This includes the potential for tendon disorders and rupture, particularly when corticosteroids are used simultaneously. This increased risk is noted in the official product information for use in this population.

Q: Are there any age restrictions for taking Azo-Ciproflox?

A: The Ciprofloxacin component is generally indicated for use in adult patients for urinary tract infections. Specific use and dosage for pediatric patients, including children, is determined based on individual regulatory guidelines and professional assessment.

Q: What does the research evidence say about Azo-Ciproflox for uncomplicated issues?

A: According to official documents, the Ciprofloxacin component of this drug is reserved for treating acute uncomplicated cystitis (a simple UTI) only when alternative treatment options are unavailable. This restriction is due to the potential risk of disabling and possibly irreversible serious adverse reactions associated with the quinolone class of drugs.

Q: Why is Azo-Ciproflox sometimes prescribed for UTIs?

A: This combination is prescribed for UTIs to offer a comprehensive, dual approach to treatment. The Ciprofloxacin component addresses the microbial infection, while the Phenazopyridine component provides immediate, local relief from uncomfortable symptoms like pain and burning in the urinary tract.

Q: What should I do if I miss a dose of Azo-Ciproflox?

A: General dosing advice described in regulatory information is that if a dose is missed, the general protocol described in dosing information is to take the missed dose as soon as possible. However, if it is almost time for the next scheduled dose, the missed dose may be skipped to prevent taking two doses too closely together.

Q: Can Azo-Ciproflox affect blood sugar levels?

A: Yes, official safety information indicates that the Ciprofloxacin component has been associated with disturbances in blood sugar regulation. This can result in either hypoglycemia (abnormally low blood sugar) or hyperglycemia (abnormally high blood sugar). This potential effect is part of the overall safety profile reviewed by healthcare providers when prescribing.

Q: Is it possible to have an allergic reaction to Azo-Ciproflox?

A: Yes, like many medications, the Ciprofloxacin component carries a risk of serious hypersensitivity reactions, including severe allergic reactions (anaphylaxis). Official guidelines state that the drug is to be discontinued at the first sign of a rash or other indication of hypersensitivity.

Q: What if I take Azo-Ciproflox and my symptoms don't improve?

A: The Ciprofloxacin component is intended to treat specific, susceptible bacterial infections. If your clinical symptoms do not improve or worsen after starting the medication, official guidelines indicate this may suggest the bacteria are resistant to the antibiotic. A healthcare provider is typically consulted to determine next steps, such as a change in treatment or definitive diagnosis.

Q: Is Azo-Ciproflox the same as the over-the-counter Azo product?

A: No, they are not the same. The prescription drug Azo-Ciproflox contains the antibiotic Ciprofloxacin plus Phenazopyridine. In contrast, the common over-the-counter Azo product typically contains Phenazopyridine alone and is only intended for symptomatic relief, not for curing an infection.

Q: Can taking Azo-Ciproflox cause sleep disturbances?

A: Official information regarding the Ciprofloxacin component mentions the potential for Central Nervous System (CNS) effects. One reported side effect observed in post-approval monitoring is insomnia (difficulty falling asleep or staying asleep).

Q: Is it okay to drink alcohol in moderation while using Azo-Ciproflox?

A: While the Ciprofloxacin component does not carry an official absolute contraindication against alcohol in its primary labeling, consuming alcohol may potentially increase the risk or severity of certain common side effects. These can include nausea, dizziness, or liver-related issues.

Q: Can Azo-Ciproflox be used during pregnancy?

A: The use of this product during pregnancy is generally cautioned. The Phenazopyridine component is contraindicated in cases of pyelonephritis (kidney infection) during pregnancy. For the Ciprofloxacin component, there are no controlled studies in human pregnancy, and is generally considered in research to be used only when the potential benefit is assessed to outweigh the potential risk.

Q: Is there a risk of C. difficile infection when taking Azo-Ciproflox?

A: Yes, regulatory documents note that Clostridium difficile-Associated Diarrhea (CDAD) has been reported with the use of nearly all antibacterial agents, including the Ciprofloxacin component. This can range in severity from mild diarrhea to a more serious intestinal condition.

Q: Does Azo-Ciproflox interact with dairy products?

A: Yes, official labeling notes that the co-ingestion of the Ciprofloxacin component with dairy products like milk or yogurt, or with calcium-fortified juices, can decrease the absorption of the antibiotic. This is a pharmacokinetic effect that can reduce the drug's effectiveness.

Q: Is Azo-Ciproflox typically prescribed for a short time?

A: Yes, the combination tablet is intended for very short-term use. Official labeling for the Phenazopyridine component states its use in conjunction with an antibacterial agent should not exceed 2 days (four doses). After this, treatment continues only with the Ciprofloxacin component.

Q: Are there specific mental health side effects noted for Azo-Ciproflox?

A: Regulatory safety information indicates that the Ciprofloxacin component may cause Central Nervous System (CNS) effects. These can include psychological symptoms such as anxiety, hallucinations, and, in rare instances, toxic psychosis.

Q: Can Azo-Ciproflox cause skin rash?

A: Yes, official product information lists skin rash as a common adverse reaction (ge 1%) for the Ciprofloxacin component. Rash is also documented as a potential side effect of the Phenazopyridine component.

Q: Does Azo-Ciproflox affect the results of laboratory tests?

A: Yes, the Phenazopyridine component is known to interfere with the accuracy of specific laboratory tests that rely on colorimetric methods for analysis, particularly urine tests. Official guidance notes that medical staff should be informed of this drug’s use before laboratory tests are performed.

Q: Are there any long-term effects of taking Azo-Ciproflox?

A: Official warnings state that the Ciprofloxacin component is associated with disabling and potentially irreversible serious adverse reactions. These reactions include effects on the tendons (e.g., rupture) and peripheral nerves (peripheral neuropathy). For these reasons, the drug is typically not used for long-term therapy.

Q: What is the chemical name for Azo-Ciproflox?

A: Azo-Ciproflox is a combination product containing two distinct compounds. The anti-infective component is Ciprofloxacin (a synthetic fluoroquinolone), and the analgesic component is Phenazopyridine Hydrochloride (an azo dye used for urinary pain relief).

Q: Do studies examine the effectiveness of the combined components of Azo-Ciproflox?

A: Official information notes that no evidence exists to show that the combined administration of Phenazopyridine and an antimicrobial provides a clinical benefit greater than the antimicrobial alone after the initial two-day period. The combination is used to address both the infection and symptoms, though the Phenazopyridine component does not enhance the antimicrobial action of Ciprofloxacin.

Q: Is Azo-Ciproflox prescribed for men as often as it is for women?

A: The Ciprofloxacin component is indicated for use in all adult patients for various infections. However, the evidence base for uncomplicated cystitis (the most common indication for this combination) primarily involves studies conducted on adult women.

Q: Can I take Azo-Ciproflox if I am breastfeeding?

A: Breastfeeding is not recommended during treatment with the Ciprofloxacin component. Official guidance suggests that a woman may pump and discard breast milk during the course of treatment and for an additional two days after the final dose.

Q: Why are people often told to drink plenty of water with Azo-Ciproflox?

A: Patients are advised to drink extra water or fluids while using the Ciprofloxacin component to help prevent crystalluria. Crystalluria is a documented side effect involving the formation of crystals in the urine and is managed by ensuring adequate hydration.

Q: Is the red/orange urine dangerous or just a side effect?

A: The reddish-orange discoloration of urine is caused by the Phenazopyridine component and is an expected, common, and temporary safety characteristic noted in official labeling. While the color change itself is not dangerous, any other unusual symptoms should still be reported to a healthcare provider.

Q: Why is there a warning about kidney stone formation with this type of drug?

A: The Ciprofloxacin component has been associated with the potential for crystalluria, which is the presence of crystals in the urine. This condition, which can be a precursor to stone formation, is typically addressed by emphasizing the need for adequate fluid intake during the course of therapy.

Q: How quickly does Azo-Ciproflox start to relieve discomfort?

A: The Phenazopyridine component is included specifically to provide immediate symptomatic relief by its topical anesthetic action on the urinary tract. While official regulatory documents do not specify a precise time-to-onset, its purpose is to offer fast relief of pain and burning.

Q: How long does the red color in urine last after stopping Azo-Ciproflox?

A: The reddish-orange discoloration of urine will typically last for a short time after the medication is discontinued, as the body works to clear the Phenazopyridine component. Regulatory documents do not provide a specific duration, but the color change should fade shortly after stopping the drug.

Q: What should I tell my healthcare provider before starting Azo-Ciproflox?

A: Regulatory guidance suggests that a healthcare provider should be informed about all medications, including prescription drugs and supplements, as the Ciprofloxacin component has many potential interactions, such as with Tizanidine and certain antacids. Additionally, disclosing any history of renal (kidney) or hepatic (liver) impairment is important, as these conditions can restrict the use of the Phenazopyridine component.

Q: Does Azo-Ciproflox have an interaction with caffeine?

A: Yes, regulatory information indicates that the Ciprofloxacin component is a known inhibitor of the CYP1A2 enzyme. This inhibition can lead to elevated plasma levels of other medicines metabolized by this pathway, including caffeine. This may result in increased effects or side effects of caffeine.

Q: What happens if I take Azo-Ciproflox but don't actually have an infection?

A: Taking the Ciprofloxacin component when no bacterial infection is present may increase the risk of certain serious adverse reactions without providing a therapeutic benefit. Official guidelines emphasize that the use of antibiotics should be reserved for the treatment of susceptible bacterial infections.


How should Azo-Ciproflox be stored and disposed of?

How to Store and Dispose of Azo-Ciproflox

Official regulatory documents define strict conditions for storing and disposing of this medication.

Required Storage and Protection

This medication must be stored at controlled room temperature, specifically between 20 C and 25 C (68 F and 77 F). The product must be kept in a dry place and protected from light to maintain stability. The medicine must always be stored out of the reach of children.

Packaging and Disposal

Ensure the packaging remains intact; do not use the medication if the blister or container is torn or damaged. Official instructions require that any unused portion of the medication be discarded after therapy is completed.

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

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