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Azithromycin
Antibiotic

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

Antibiotic

Azithromycin

Azithromycin is a vital Active Pharmaceutical Ingredient (API) belonging to the Macrolide Antibiotics class. It is characterized by its broad spectrum of activity against a wide range of Gram-positive and Gram-negative bacteria, in addition to its unique pharmacokinetic profile that enables short dosing regimens. We supply Azithromycin with high quality and purity, ideal for the production of tablets, capsules, suspensions, and extended-release 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:
Macrolide Antibiotic.
Mechanism of Action:
Inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit of the bacteria, thereby preventing peptidyl transfer.
Clinical Application:
Treatment of respiratory tract infections (e.g., pneumonia, bronchitis), middle ear infections (otitis media), skin and soft tissue infections, and certain sexually transmitted diseases.
Competitive Advantage:
Azithromycin possesses a long half-life and accumulates at high concentrations in tissues, allowing for short treatment courses (typically 3 to 5 days).
Tablets and Capsules

Immediate-release tablets and capsules.

Offers good powder flow and compressibility characteristics, essential for high-speed tableting and encapsulation processes.

Liquid Suspensions

Oral suspensions for pediatric use..

Supplied in a form that facilitates the preparation of stable, homogeneous suspensions, with the need to address the inherent bitterness during formulation.

Extended-Release Formulations

Extended-release suspensions or tablets (e.g., Z-Pak/Zithromax extended-release).

Ideal for complex formulations requiring slow and controlled release of the active ingredient.

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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