Description

Tetracycline Hydrochloride USP

Tetracycline Hydrochloride USP is a high-purity, broad-spectrum antibiotic used in pharmaceutical formulations for the treatment of bacterial infections caused by gram-positive and gram-negative organisms. Compliant with United States Pharmacopeia (USP) standards, it functions by inhibiting bacterial protein synthesis through binding to the 30S ribosomal subunit, preventing the addition of amino acids to growing peptide chains. Tetracycline Hydrochloride is
• A USP-compliant tetracycline-class antibiotic for oral, topical, and parenteral formulations
• Effective against a broad range of bacterial pathogens
• Used in tablets, capsules, ointments, and injectable dosage forms
• Suitable for respiratory, urinary, gastrointestinal, and skin infections
• Manufactured under Good Manufacturing Practice (GMP) certified conditions
• Supplied with complete regulatory documentation including Certificate of Analysis (CoA) and technical data
Tetracycline Hydrochloride is chemically designated as (4S,4aS,5aR,6S,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride. It appears as a yellow to yellow-orange crystalline powder, soluble in water and alcohols, and stable under controlled storage conditions.
In pharmaceutical applications, Tetracycline Hydrochloride USP is used in:
• Oral tablets and capsules for systemic infections and acne therapy
• Topical creams and ointments for dermatological infections and wound care
• Parenteral formulations for severe or resistant bacterial infections
• Veterinary medicine and research for antimicrobial testing
• Combination therapies with other antibiotics for synergistic effects
Tetracycline Hydrochloride USP demonstrates reliable absorption, distribution, and efficacy against a wide variety of microorganisms. Its well-established safety profile and broad activity spectrum make it a key antibiotic in both human and veterinary medicine.
CarboMer supplies Tetracycline Hydrochloride USP with control over assay, potency, residual solvents, and microbial purity. Material meets USP monograph standards and is suitable for regulated pharmaceutical applications.
The material is packaged in sealed, moisture-protective, tamper-evident containers. Available in laboratory, pilot, and commercial-scale volumes. Minimum order quantities (MOQ), lead times, and documentation, including CoA and SDS, are provided upon request.
Each batch is tested for identity (IR, HPLC), potency, water content, residual solvents, pH, and microbial limits. Certificates of Analysis (CoA), Safety Data Sheets (SDS), and full traceability documentation accompany every shipment.
As with all CarboMer antibiotic APIs, Tetracycline Hydrochloride USP is supported by formulation expertise, regulatory guidance, and dependable global supply to ensure safe, effective, and compliant pharmaceutical products.