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Amoxicilin
Antibiotic

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

Antibiotic

Amoxicilin

Amoxicillin is a core Active Pharmaceutical Ingredient (API) belonging to the Broad-Spectrum Penicillin Antibiotics class. It is one of the most widely used antibiotics globally due to its excellent oral bioavailability and effectiveness against a large range of Gram-positive and Gram-negative bacteria. We supply Amoxicillin (typically in its Trihydrate form) with high quality and optimal purity to support the production of capsules, chewable tablets, and pediatric suspensions.

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 Semisynthetic Penicillin Antibiotic.
Mechanism of Action:
Inhibits bacterial cell wall synthesis by binding to Penicillin-Binding Proteins (PBPs), ultimately leading to cell wall breakdown and bacteriolysis.
Clinical Application:
Treatment of respiratory tract infections, otitis media, sinusitis, skin infections, and urinary tract infections. Often used in combination with Beta-lactamase inhibitors (e.g., Clavulanic Acid).
Competitive Advantage:
Possesses a higher oral absorption rate than Ampicillin, making it the preferred choice for oral formulations.
Capsules and Tablets

Immediate-release capsules and chewable tablets.

Offers uniform flow and compressibility characteristics, which are vital for high-speed filling and compression processes.

Pediatric Suspensions

Powder for oral suspensions.

Amoxicillin is provided in a suitable form for granulation and dry blending processes, yielding a stable suspension powder that is easy for patients to reconstitute.

Combined Formulations

Tablets or suspensions containing Amoxicillin and Clavulanic Acid.

Excellent compatibility with Clavulanic Acid (while observing stringent moisture precautions) for manufacturing stable, broad-spectrum combination drugs.

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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