Cefpodoxime Proxetil Powder

Cefpodoxime Proxetil Powder - High-Quality API CAS No.: 80210-62-4 Molecular Weight: 557.6 g/mol Chemical Formula: C21H27N5O9S2 Form: Fine crystalline powder, off-white to pale yellow Product Overview Cefpodoxime Proxetil Powder is a third-generation cephalosporin antibiotic active pharmaceutical ingredient (API). It is supplied as a high-purity, stable powder, manufactured under stringent GMP standards to meet global pharmacopeial requirements. Known for its excellent bioavailability and broad antibacterial spectrum, Cefpodoxime Proxetil is widely used in the formulation of oral dosage forms. Key Applications Pharmaceutical Formulations: Used in the preparation of tablets, dry syrups, and capsules for systemic treatment of bacterial infections. Indicated for respiratory tract infections, urinary tract infections, skin and soft tissue infections, and certain ENT (ear, nose, throat) infections. Research & Development: Suitable for analytical studies, microbiological research, and development of new dosage forms. Specifications & Quality Appearance: Off-white to pale yellow crystalline powder Assay (on anhydrous basis): ≥ 98% Solubility: Practically insoluble in water; soluble in methanol and certain organic solvents Packaging: Available in HDPE drums or fiber containers with double polyethylene liners, ranging from 1 kg to 25 kg All batches undergo rigorous testing for purity, potency, and stability to ensure consistent performance in final formulations. Advantages Broad-spectrum antibacterial activity against Gram-positive and Gram-negative organisms Excellent oral absorption after conversion to the active form, cefpodoxime Long shelf life when stored in recommended conditions Storage & Handling Store in a cool, dry place, away from direct sunlight and moisture. Recommended storage temperature: below 25°C. Keep container tightly closed when not in use. Precautions For industrial and pharmaceutical use only. Not intended for direct human consumption. Handle with gloves, protective clothing, and safety goggles to avoid skin or eye contact. Avoid inhalation of dust; use in a well-ventilated area or under fume extraction. Dispose of waste material as per local environmental regulations. Consult the Safety Data Sheet (SDS) before handling large quantities. Compliance & Certifications Manufactured under WHO-GMP / ISO-certified facilities Follows pharmacopeial standards (USP/BP/EP) Note: This information is for reference and technical use by qualified professionals. End users must validate the material's suitability for their intended applications. About the Company GST Registration Date: 2024 Legal Status of Firm: Partnership Number of Employees: 11 To 25 People Annual Turnover: 0 - 40 L