USP Standard Fluorometholone API with US DMF 36772 and EU GMP Certified Synthetic Glucocorticoid for Ophthalmic Use
US DMF 36772 Fluorometholone API
,USP Standard Fluorometholone
,EU GMP Certified Synthetic Glucocorticoid
Original Manufacturer: Henan Lihua Pharmaceutical Co., Ltd.CEP: Not Available Chinese CDE Registration: Y20250000004 — Status “I” EU GMP Status: Certified by EMA FDA Inspection Status: NAI (July 2021) Standard: USP Annual Capacity: Please contact us for details Disclaimer: All detailed product ...
Original Manufacturer: Henan Lihua Pharmaceutical Co., Ltd.
CEP: Not Available
Chinese CDE Registration: Y20250000004 — Status “I”
EU GMP Status: Certified by EMA
FDA Inspection Status: NAI (July 2021)
Standard: USP
Annual Capacity: Please contact us for details
Disclaimer: All detailed product information shall be subject to the issued final COA. US DMF Letters of Authorization (LOA) are available to qualified buyers upon request. The Chinese CDE registration status for this product is currently “I” (not yet linked with an approved formulation); buyers requiring Chinese market eligibility should contact us to discuss availability and regulatory pathway. CEP is not available for this product.
USP/EP/AJI Pharmaceutical Grade L-Arginine API and Amino Acid with Cell Culture Grade Purity
Original Manufacturer: Shantou Jiahe Biotechnology Co., Ltd.Product Grade: Cell Culture Grade / Food Grade / Pharmaceutical Grade Chinese Registration: Y20180001301 (API) Certifications: GMP, ISO9001, ISO14001 Annual Capacity: Please contact us for details Package: 25 kg / Drum Disclaimer: All ...
Original Manufacturer Epirubicin HCl Anthracycline Compound with US DMF 19818 and USP EP BP JP Standard
Original Manufacturer: Shandong New Time Pharmaceutical Co., Ltd.US DMF: Active — DMF 19818 CEP: Not Available for Epirubicin EU GMP Status: Company holds EU GMP certification FDA Inspection Status: VAI (July 2024) Standard: USP / EP / BP / JP Annual Capacity: Please contact us for details ...
Bleomycin Sulfate Glycopeptide Compound with CEP 2025-187 and US DMF 42629 Meeting USP EP Standard
Original Manufacturer: Hubei Honch Pharmaceutical Co., Ltd.CEP: Available — CEP 2025-187 - Rev 00, Valid (issued 2026-09-02) US DMF: Active — DMF 42629 (Type II, latest filing Nov 2025) FDA Inspection Status: VAI (March 2025) EU GMP / WC: Available — EU Written Confirmation on record Standard: USP / ...
US DMF Abiraterone Acetate API and CYP17 Inhibitor Oncology Ingredient from Original Manufacturer
Original Manufacturer: Shandong Anhong Pharmaceutical Co., Ltd.Chinese CDE Registration: Y20180000623 — API US DMF: Active — Available for AbirateroneCEP: Please contact us for detailsEU GMP Status: Company holds EU GMP certification FDA Inspection Status: OAI (June 2026)Standard: Please contact us ...
