Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Reset all filters
01 1Farmak A.S. Olomouc CZ
02 1SANOFI WINTHROP INDUSTRIE Gentilly FR
03 1AARTI DRUGS LIMITED Mumbai IN
04 1ALIVUS LIFE SCIENCES LIMITED Mumbai IN
05 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
06 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
07 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
08 1CIPLA LIMITED Mumbai IN
09 1Cambrex Profarmaco Milano S.r.l. Paullo IT
10 1LAKE CHEMICALS PRIVATE LIMITED Bengaluru IN
11 1LUPIN LIMITED Mumbai IN
12 1MATRIX PHARMACORP PRIVATE LIMITED Sangareddy District IN
13 2SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
14 1SYNTHON BV Nijmegen NL
15 1TAPI NL B.V. Amsterdam NL
16 1UNICHEM LABORATORIES LIMITED Mumbai IN
17 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
18 1Uquifa Mexico S.A. de C.V. Jiutepec MX
Reset all filters
01 19Zolpidem tartrate
02 1Zolpidem tartrate, Site-II
Reset all filters
01 1Czech Republic
02 1France
03 12India
04 1Netherlands
05 2Spain
06 1U.S.A
07 2Blank
Reset all filters
01 1Expired
02 16Valid
03 3Withdrawn by Holder
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Certificate Number : CEP 2000-319 - Rev 06
Status : Valid
Issue Date : 2025-03-28
Type : Chemical
Substance Number : 1280
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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
Certificate Number : CEP 2007-102 - Rev 05
Status : Valid
Issue Date : 2025-04-14
Type : Chemical
Substance Number : 1280
Certificate Number : R1-CEP 2005-035 - Rev 04
Status : Valid
Issue Date : 2020-11-27
Type : Chemical
Substance Number : 1280
Certificate Number : CEP 2002-171 - Rev 07
Status : Valid
Issue Date : 2025-06-25
Type : Chemical
Substance Number : 1280
Certificate Number : CEP 2018-022 - Rev 02
Status : Valid
Issue Date : 2025-07-29
Type : Chemical
Substance Number : 1280
Certificate Number : R1-CEP 2006-032 - Rev 01
Status : Valid
Issue Date : 2016-09-13
Type : Chemical
Substance Number : 1280
Certificate Number : CEP 2005-067 - Rev 03
Status : Valid
Issue Date : 2025-08-08
Type : Chemical
Substance Number : 1280
Certificate Number : CEP 2008-153 - Rev 01
Status : Valid
Issue Date : 2024-11-07
Type : Chemical
Substance Number : 1280
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2006-293 - Rev 08
Status : Valid
Issue Date : 2025-09-16
Type : Chemical
Substance Number : 1280
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
63
PharmaCompass offers a list of Zolpidem Tartrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Zolpidem Tartrate manufacturer or Zolpidem Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zolpidem Tartrate manufacturer or Zolpidem Tartrate supplier.
PharmaCompass also assists you with knowing the Zolpidem Tartrate API Price utilized in the formulation of products. Zolpidem Tartrate API Price is not always fixed or binding as the Zolpidem Tartrate Price is obtained through a variety of data sources. The Zolpidem Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cymerion manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cymerion, including repackagers and relabelers. The FDA regulates Cymerion manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cymerion 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 Cymerion manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cymerion supplier is an individual or a company that provides Cymerion active pharmaceutical ingredient (API) or Cymerion finished formulations upon request. The Cymerion suppliers may include Cymerion API manufacturers, exporters, distributors and traders.
click here to find a list of Cymerion suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cymerion CEP of the European Pharmacopoeia monograph is often referred to as a Cymerion Certificate of Suitability (COS). The purpose of a Cymerion CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cymerion EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cymerion to their clients by showing that a Cymerion CEP has been issued for it. The manufacturer submits a Cymerion CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cymerion CEP holder for the record. Additionally, the data presented in the Cymerion CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cymerion DMF.
A Cymerion CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cymerion 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 Cymerion suppliers with CEP (COS) on PharmaCompass.
We have 15 companies offering Cymerion
Get in contact with the supplier of your choice: