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Lencomycin
Antibiotic

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

Antibiotic

Lencomycin

Lincomycin is a foundational antibiotic belonging to the Lincosamides class. It is characterized by its directed effectiveness against a wide spectrum of Gram-positive aerobic and anaerobic bacteria, including common pathogens like Staphylococci and Streptococci. We supply Lincomycin in its Hydrochloride (HCl) salt form, which features high water solubility, making it ideal for injectable and liquid oral formulations, including both human and veterinary applications.

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:
Lincosamide Antibiotic.
Mechanism of Action:
Inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit of the bacteria, the same binding site as macrolides.
Clinical Application:
Treatment of serious infections caused by susceptible bacteria, such as bone and joint infections, respiratory tract infections, and skin and soft tissue infections.
Competitive Advantage:
A highly effective API often used as an alternative for patients with penicillin hypersensitivity or in cases of infections resistant to macrolides.
Injectables

Sterile solutions for intramuscular (IM) or intravenous (IV) injection (for both human and veterinary use).

The high solubility of the HCl salt and the availability of high-purity grades meet strict sterility requirements.

Tablets and Capsules

Oral tablets and capsules.

Good powder flow and compressibility characteristics for standard tableting and filling processes.

Liquid Formulations

Oral solutions and syrups (especially for veterinary use).

Excellent stability in aqueous solutions, facilitating the manufacture of liquid products with long shelf lives.

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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