Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica
02 1SCI Pharmtech
03 1TAPI Technology & API Services
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05 2Alembic Pharmaceuticals Limited
06 1Alkem Laboratories
07 2Aurobindo Pharma Limited
08 1CTX Lifesciences
09 1Cadila Pharmaceuticals
10 1Chongqing Shenghuaxi Pharma. Co., Ltd
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12 1Esteve Quimica
13 1HEC Pharm
14 1Hansoh Pharma
15 1Hetero Drugs
16 1Jubilant Generics
17 1Liaoyuan Pharmaceutical
18 2Lupin Ltd
19 1MATRIX LABORATORIES XIAMEN LTD.
20 2MSN Laboratories
21 2Macleods Pharmaceuticals Limited
22 1Nosch Labs Pvt
23 1Olon S.p.A
24 1Orchid Pharma
25 1R L Fine Chem
26 1RANBAXY LABORATORIES LIMITED
27 1Shanghai Wonder Pharmaceutical
28 1Shodhana Laboratories Pvt. Ltd
29 1Signa S.A. de C.V.
30 1Sun Pharmaceutical Industries Limited
31 1Torrent Pharmaceuticals Limited
32 1Viatris
33 1Wockhardt
34 1Zhejiang Huahai Pharmaceutical
35 1Zhejiang Jiuzhou Pharmaceutical
36 1Zhejiang Yongtai Technology
37 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
A Duloxetine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duloxetine, including repackagers and relabelers. The FDA regulates Duloxetine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duloxetine 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 Duloxetine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duloxetine supplier is an individual or a company that provides Duloxetine active pharmaceutical ingredient (API) or Duloxetine finished formulations upon request. The Duloxetine suppliers may include Duloxetine API manufacturers, exporters, distributors and traders.
click here to find a list of Duloxetine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Duloxetine DMF (Drug Master File) is a document detailing the whole manufacturing process of Duloxetine active pharmaceutical ingredient (API) in detail. Different forms of Duloxetine DMFs exist exist since differing nations have different regulations, such as Duloxetine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Duloxetine DMF submitted to regulatory agencies in the US is known as a USDMF. Duloxetine USDMF includes data on Duloxetine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Duloxetine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Duloxetine suppliers with USDMF on PharmaCompass.
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