Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1FARMAK, a.s
02 1Veranova
03 1Enaltec Labs
04 1Aurobindo Pharma Limited
05 1Biddle Sawyer Corporation
06 1Emcure Pharmaceuticals
07 1Industriale Chimica
08 1Intas Pharmaceuticals
09 1Kaken Pharmaceuticals
10 1MSN Laboratories
11 1Sigmapharm Laboratories, LLC
12 1Sun Pharmaceutical Industries Limited
13 1Viatris
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
GDUFA
DMF Review : Complete
Rev. Date : 2018-04-06
Pay. Date : 2017-10-02
DMF Number : 31858
Submission : 2017-07-24
Status :
Type : II
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : Complete
Rev. Date : 2014-07-18
Pay. Date : 2014-02-12
DMF Number : 27816
Submission : 2014-02-25
Status :
Type : II
Enaltec Labs –Delivering complex APIs with precision, innovation, and global compliance.
GDUFA
DMF Review : Complete
Rev. Date : 2018-10-16
Pay. Date : 2018-05-29
DMF Number : 31939
Submission : 2018-05-30
Status :
Type : II
58
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A Tox21_112178 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_112178, including repackagers and relabelers. The FDA regulates Tox21_112178 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_112178 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 Tox21_112178 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_112178 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_112178 DMFs exist exist since differing nations have different regulations, such as Tox21_112178 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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We have 13 companies offering Tox21_112178
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