 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.
 
										

 
				
									 
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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
									 
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01 19Zolpidem tartrate
02 1Zolpidem tartrate, Site-II
									 
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01 1Czech Republic
02 1France
03 12India
04 1Netherlands
05 2Spain
06 1U.S.A
07 2Blank
									 
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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.
 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.
 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
 Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.                    
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 Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.                    
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												Certificate Number : R1-CEP 2007-222 - Rev 00
Status : Valid
Issue Date : 2014-07-25
Type : Chemical
Substance Number : 1280

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												Certificate Number : R1-CEP 2005-035 - Rev 04
Status : Valid
Issue Date : 2020-11-27
Type : Chemical
Substance Number : 1280

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												Certificate Number : CEP 2002-171 - Rev 07
Status : Valid
Issue Date : 2025-06-25
Type : Chemical
Substance Number : 1280

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												Certificate Number : CEP 2018-022 - Rev 02
Status : Valid
Issue Date : 2025-07-29
Type : Chemical
Substance Number : 1280

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												Certificate Number : R1-CEP 2006-032 - Rev 01
Status : Valid
Issue Date : 2016-09-13
Type : Chemical
Substance Number : 1280

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												Certificate Number : CEP 2008-153 - Rev 01
Status : Valid
Issue Date : 2024-11-07
Type : Chemical
Substance Number : 1280

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												Certificate Number : R1-CEP 2003-144 - Rev 03
Status : Valid
Issue Date : 2020-06-17
Type : Chemical
Substance Number : 1280

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF

 
												 
												Certificate Number : CEP 2004-159 - Rev 05
Status : Valid
Issue Date : 2025-02-03
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 Zolpimist manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolpimist, including repackagers and relabelers. The FDA regulates Zolpimist manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolpimist 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 Zolpimist manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolpimist supplier is an individual or a company that provides Zolpimist active pharmaceutical ingredient (API) or Zolpimist finished formulations upon request. The Zolpimist suppliers may include Zolpimist API manufacturers, exporters, distributors and traders.
click here to find a list of Zolpimist suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zolpimist CEP of the European Pharmacopoeia monograph is often referred to as a Zolpimist Certificate of Suitability (COS). The purpose of a Zolpimist CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zolpimist EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zolpimist to their clients by showing that a Zolpimist CEP has been issued for it. The manufacturer submits a Zolpimist CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zolpimist CEP holder for the record. Additionally, the data presented in the Zolpimist CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zolpimist DMF.
A Zolpimist CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zolpimist 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 Zolpimist suppliers with CEP (COS) on PharmaCompass.
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