Korea MFDS Certified CDE Status A Microcirculation Ingredient Calcium Dobesilate Monohydrate API
Korea MFDS Certified Calcium Dobesilate
,CDE Status A Calcium Dobesilate Monohydrate
,Microcirculation Ingredient Calcium Dobesilate
Original Manufacturer: Hubei Guangchen Pharmaceutical Co., Ltd.Korea MFDS: Certified (on-site inspection passed, 2018) CEP: Please contact us for details US DMF: Please contact us for details Production License Scope: “For Registration Filing Use” Standard: ChP / EP / BP Disclaimer: All detailed ...
Original Manufacturer: Hubei Guangchen Pharmaceutical Co., Ltd.
Korea MFDS: Certified (on-site inspection passed, 2018)
CEP: Please contact us for details
US DMF: Please contact us for details
Production License Scope: “For Registration Filing Use”
Standard: ChP / EP / BP
Disclaimer: All detailed product information shall be subject to the issued final COA. The Chinese production license scope for this product is currently “For Registration Filing Use”; buyers requiring commercial-scale supply should contact us to discuss availability and batch documentation. CEP and US DMF status specific to Calcium Dobesilate Monohydrate must be confirmed with our team before relying on any regulatory filing pathway.
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 ...
