Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak A.S. Olomouc CZ
02 1SANOFI WINTHROP INDUSTRIE Gentilly FR
03 1AARTI DRUGS LIMITED Mumbai IN
04 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
05 1BACHEM S.A. Vionnaz CH
06 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
07 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
08 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
09 1CIPLA LIMITED Mumbai IN
10 1Cambrex Profarmaco Milano S.r.l. Paullo IT
11 1DIVI'S LABORATORIES LIMITED Hyderabad IN
12 1GLENMARK LIFE SCIENCES LIMITED Mumbai IN
13 1LAKE CHEMICALS PRIVATE LIMITED Bengaluru IN
14 1LUPIN LIMITED Mumbai IN
15 2SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
16 1SYNTHON BV Nijmegen NL
17 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
18 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
19 1Unichem Laboratories Limited Mumbai IN
20 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
21 1Uquifa Mexico S.A. de C.V. Jiutepec MX
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Certificate Number : CEP 2000-319 - Rev 05
Status : Valid
Issue Date : 2024-02-02
Type : Chemical
Substance Number : 1280
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : CEP 2001-071 - Rev 05
Status : Valid
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 1280
A Zolpidem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolpidem, including repackagers and relabelers. The FDA regulates Zolpidem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolpidem API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Zolpidem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolpidem supplier is an individual or a company that provides Zolpidem active pharmaceutical ingredient (API) or Zolpidem finished formulations upon request. The Zolpidem suppliers may include Zolpidem API manufacturers, exporters, distributors and traders.
click here to find a list of Zolpidem suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zolpidem CEP of the European Pharmacopoeia monograph is often referred to as a Zolpidem Certificate of Suitability (COS). The purpose of a Zolpidem CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zolpidem EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zolpidem to their clients by showing that a Zolpidem CEP has been issued for it. The manufacturer submits a Zolpidem CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zolpidem CEP holder for the record. Additionally, the data presented in the Zolpidem CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zolpidem DMF.
A Zolpidem CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zolpidem CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Zolpidem suppliers with CEP (COS) on PharmaCompass.
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