Pipemidic Acid, Pipemidic Acid API, Anhydrous, Trihydrate, Quinolone Compound, Shandong Xinhua, JDMF, EU-WC, CAS No. 51940-44-4
Original Manufacturer: Shandong Xinhua Pharmaceutical Co., Ltd.EU Regulatory Record: Approved as API source in Italian AIFA-authorized finished product (2015) International Filings: USDMF, CEP/COS, JDMF, EU-WC registered Standard: USP / EP / BP / JP / ChP Annual Capacity: Please contact us for ...
Original Manufacturer: Shandong Xinhua Pharmaceutical Co., Ltd.
EU Regulatory Record: Approved as API source in Italian AIFA-authorized finished product (2015)
International Filings: USDMF, CEP/COS, JDMF, EU-WC registered
Standard: USP / EP / BP / JP / ChP
Annual Capacity: Please contact us for details
Disclaimer: All detailed product information shall be subject to the issued final COA. Regulatory documentation (e.g., ASMF/DMF references, CEP copies) is available to qualified buyers upon request. Please contact us with your target market and required hydrate form.
Acarbose, Acarbose API, Glucobay, Alpha-Glucosidase Inhibitor, CSPC Shengxue, CEP 2011-054, US DMF 35603, CAS No. 56180-94-0
Original Manufacturer: CSPC Shengxue Glucose Co., Ltd. (CSPC Pharmaceutical Group) CEP: Available — R1-CEP 2011-054 US DMF: Available — DMF 35603 EU GMP Certificate: Issued by Germany (March 2024) FDA Inspection Status: NAI (2024) Standard: USP / EP / ChP / JP Annual Capacity: Please contact us for ...
Sevoflurane API, Inhalation Agent, Volatile Liquid, Shandong New Time, Lunan Pharmaceutical, CEP 2012-234, US DMF 22740, USP/EP standard, CAS No. 28523-86-6
Original Manufacturer: Shandong New Time Pharmaceutical Co., Ltd. (Lunan Pharmaceutical Group)CDA No.: H20080680 (API)CEP: Available — CEP 2012-234 (Rev 01, valid)US DMF: Available — DMF 22740 (Type II, Status A)FDA Regulatory Status: Referenced in an approved ANDA for Sevoflurane Inhalation ...
Citicoline Sodium, CDP-Choline, Citicoline Sodium API, Nucleoside API, Xinxiang Pharmaceutical, USP/EP standard, Neuroprotective agent, CAS No. 33818-15-4
Original Manufacturer: Xinxiang Pharmaceutical Co., Ltd. CDE Registration Status: A GMP Status: Compliant (Issued January 2026) Standard: ChP / USP / EP CEP: Not Applicable International DMF Filings: Available in selected markets (e.g., India, Uzbekistan) Annual Capacity: Please contact us for ...
Allopurinol, Zyloprim, USP/EP/BP grade, Huangshi Pharma, Xanthine oxidase inhibitor, Gout treatment API, CAS No. 315-30-0
Original Manufacturer: Huangshi Pharma Co., Ltd. (Huangshi Fam Pharmaceutical)DMF: Available / Not Available CEP: Under Preparation WC (Written Confirmation): N/AStandard: USP / EP / BPAnnual Capacity: 500 MT Disclaimer: All detailed product information shall be subject to the issued final COA. ...
