Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1FARMAK, a.s
02 1Sanofi
03 2TAPI Technology & API Services
04 1Aarti Drugs
05 2Alivus Life Sciences
06 1Aurobindo Pharma Limited
07 1Cadila Pharmaceuticals
08 1Cambrex Corporation
09 1Centaur Pharmaceuticals
10 1Cipla
11 1Divis Laboratories
12 1Gador SA
13 2Lunan Pharmaceutical
14 1Lupin Ltd
15 1Orchid Pharma
16 1Quimica Sintetica
17 1SYNTHON Chemicals GmbH & Co. KG
18 2Sun Pharmaceutical Industries Limited
19 1Synthelabo Tanabe Chimie
20 1Torrent Pharmaceuticals Limited
21 1UQUIFA
22 1Unichem Laboratories Limited
23 1Viatris
24 1Wockhardt
25 1YUNG ZIP CHEMICAL INDUSTRIAL
26 1Zentiva
27 1Zydus Lifesciences
28 1Blank
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
GDUFA
DMF Review : Complete
Rev. Date : 2019-04-11
Pay. Date : 2019-04-05
DMF Number : 15486
Submission : 2001-06-21
Status :
Type : II
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20984
Submission : 2007-10-30
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-24
Pay. Date : 2012-11-13
DMF Number : 15958
Submission : 2002-04-29
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18982
Submission : 2005-11-28
Status :
Type : II
63
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A AMBIEN CR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AMBIEN CR, including repackagers and relabelers. The FDA regulates AMBIEN CR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AMBIEN CR API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A AMBIEN CR DMF (Drug Master File) is a document detailing the whole manufacturing process of AMBIEN CR active pharmaceutical ingredient (API) in detail. Different forms of AMBIEN CR DMFs exist exist since differing nations have different regulations, such as AMBIEN CR USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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We have 27 companies offering AMBIEN CR
Get in contact with the supplier of your choice:
