Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica
02 1SCI Pharmtech
03 1TAPI Technology & API Services
04 1Ajanta Pharma Limited
05 2Alembic Pharmaceuticals Limited
06 1Alkem Laboratories
07 2Aurobindo Pharma Limited
08 1CTX Lifesciences
09 1Cadila Pharmaceuticals
10 1Chongqing Shenghuaxi Pharma. Co., Ltd
11 1Erregierre SpA
12 1Esteve Quimica
13 1HEC Pharm
14 1Hansoh Pharma
15 1Hetero Drugs
16 1Jubilant Generics
17 1Liaoyuan Pharmaceutical
18 2Lupin Ltd
19 2MSN Laboratories
20 2Macleods Pharmaceuticals Limited
21 1Nosch Labs Pvt
22 1Olon S.p.A
23 1Orchid Pharma
24 1R L Fine Chem
25 1Shanghai Wonder Pharmaceutical
26 1Shodhana Laboratories Pvt. Ltd
27 1Signa S.A. de C.V.
28 2Sun Pharmaceutical Industries Limited
29 1Torrent Pharmaceuticals Limited
30 1Viatris
31 1Wockhardt
32 1Zhejiang Huahai Pharmaceutical
33 1Zhejiang Jiuzhou Pharmaceutical
34 1Zhejiang Yongtai Technology
35 3Zydus Lifesciences
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : Complete
Rev. Date : 2022-04-15
Pay. Date : 2022-03-08
DMF Number : 36834
Submission : 2022-03-16
Status :
Type : II
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-23
Pay. Date : 2013-03-06
DMF Number : 24939
Submission : 2011-05-06
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 : 2012-11-23
Pay. Date : 2012-11-08
DMF Number : 21827
Submission : 2008-07-28
Status :
Type : II
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A Cymbalta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cymbalta, including repackagers and relabelers. The FDA regulates Cymbalta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cymbalta 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 Cymbalta DMF (Drug Master File) is a document detailing the whole manufacturing process of Cymbalta active pharmaceutical ingredient (API) in detail. Different forms of Cymbalta DMFs exist exist since differing nations have different regulations, such as Cymbalta USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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