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Gentamicin
Antibiotic

To guarantee the highest purity and efficacy, we adhere to strict global standards

Gentamicin

Gentamicin

Gentamicin Sulfate is a vital broad-spectrum antibiotic belonging to the Aminoglycoside class. Our product is manufactured to the highest standards of purity and potency. It is an indispensable active substance for treating serious, susceptible bacterial infections, utilized across a wide spectrum of human and veterinary pharmaceutical formulations.

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).
A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.
A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.
Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).
Therapeutic Class:
Broad-Spectrum Aminoglycoside Antibiotic.
Mechanism of Action:
Inhibits bacterial protein synthesis by critically binding to the 30S ribosomal subunit, ensuring a potent bactericidal effect.
Antibacterial Spectrum:
Highly effective against aerobic Gram-negative bacteria (including Pseudomonas aeruginosa) and certain susceptible Gram-positive strains.
Primary Indications:
Severe systemic infections, Sepsis, complicated urinary tract infections (UTIs), respiratory infections, and topical cutaneous/ocular infections.
Parenteral

Preparation of sterile solutions for Intravenous (IV) and Intramuscular (IM) injection.

Extremely high purity grade and optimal dissolution characteristics, ensuring safe and sterile preparation.

Topical

Creams, ointments, and dermal lotions.

Demonstrates stable efficacy within various dermatological base formulations.

Ophthalmic/Otic

Sterile eye drops and ear solutions.

Supplied in grades that meet stringent sterility requirements for delicate applications.

Regulatory Compliance

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).

Certificate of Analysis (CoA)

A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.

Drug Master File (DMF)

A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.

Manufacturing Operations

Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).

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