Overview of Doxylin 50%
Quick Facts
| Property | Description |
|---|---|
| Active ingredient | Doxycycline (as hyclate or monohydrate) |
| Form | Oral solid dosage form (tablet or capsule) |
| Pharmacological class | Tetracycline Antibiotic |
| General purpose | Resolving bacterial and parasitic infections |
| Origin | Semisynthetic derivative |
Defining Doxylin 50%: Classification and Purpose
Doxylin 50% is a prescription-only medication classified as a semisynthetic tetracycline antibiotic intended for the management of infections caused by susceptible microorganisms. Its general purpose is to act as a broad-spectrum bacteriostatic agent, effectively stopping the growth of a wide range of bacterial species and certain parasites. This medicine is clinically recognized for its effectiveness in containing microbial spread by preventing bacteria from multiplying. The core active ingredient, Doxycycline, places this preparation within the second generation of the tetracycline pharmacological class, which is widely valued for its reliable and versatile utility against numerous types of bacterial infections. It is recognized for its efficacy against various common pathogenic bacteria, positioning Doxylin as an established tool for fighting the microbial growth that causes infection.
Composition, Origin, and Form
The medicinal action of Doxylin 50% is derived entirely from its single active component, Doxycycline, which is typically prepared as the salt doxycycline hyclate or monohydrate. A key differentiating factor for Doxycycline among tetracyclines is its high lipid solubility, which contributes to its superior absorption profile. Doxycycline is factually categorized as a semisynthetic derivative, meaning the substance is chemically synthesized from a precursor compound naturally found within the Streptomyces bacterial genus. The "50%" designation refers specifically to the strength or concentration of the active substance within the final formulation. Doxylin 50% is typically provided as an oral solid dosage form, such as a film-coated tablet or capsule, and is designed solely for oral administration. The selection of excipients and the delivery system are engineered to ensure the stability and proper bioavailability of the active substance within the gastrointestinal tract.
Regulatory References
