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Moehs Group, a reference company in the production of pharmaceutical active ingredients. 
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01 Moehs Iberica (1)
02 RANBAXY LABORATORIES LIMITED (1)
03 Sun Pharmaceutical Industries Limited (1)
04 R L Fine Chem (1)
05 Shodhana Laboratories Pvt. Ltd (1)
06 Teva API (1)
07 Ajanta Pharma Limited (1)
08 Alembic Pharmaceuticals Limited (2)
09 Alkem Laboratories (1)
10 Aurobindo Pharma Limited (2)
11 CTX Lifesciences (1)
12 Cadila Pharmaceuticals (1)
13 Chongqing Shenghuaxi Pharma. Co., Ltd (1)
14 Erregierre SpA (1)
15 Esteve Quimica (1)
16 HEC Pharm (1)
17 Hansoh Pharma (1)
18 Hetero Drugs (1)
19 Jubilant Generics (1)
20 Lupin Ltd (2)
21 MATRIX LABORATORIES XIAMEN LTD. (1)
22 MSN Laboratories (2)
23 Macleods Pharmaceuticals Limited (2)
24 Nosch Labs Pvt. Ltd. (1)
25 Olon S.p.A (1)
26 Orchid Pharma (1)
27 SCI PHARMTECH (2)
28 Shanghai Wonder Pharmaceutical (1)
29 Signa S.A. de C.V. (1)
30 Torrent Pharmaceuticals Limited (1)
31 Viatris (1)
32 Wockhardt (1)
33 Zhejiang Huahai Pharmaceutical (1)
34 Zhejiang Jiuzhou Pharmaceutical (1)
35 Zhejiang Liaoyuan Pharmaceutical Co LTD (1)
36 Zhejiang Yongtai Technology (1)
37 Zydus Lifesciences (3)
01 DULOXETINE HCL (1)
02 DULOXETINE HCL DRUG SUBSTANCE (1)
03 DULOXETINE HYDROCHLORIDE (14)
04 DULOXETINE HYDROCHLORIDE (FROM (S)-MMAA-OME) (1)
05 DULOXETINE HYDROCHLORIDE (NON-STERILE BULK API) (1)
06 DULOXETINE HYDROCHLORIDE DELAYED-RELEASE PELLETS (1)
07 DULOXETINE HYDROCHLORIDE DRUG SUBSTANCE (1)
08 DULOXETINE HYDROCHLORIDE EP-USP (1)
09 DULOXETINE HYDROCHLORIDE NON-STERILE BULK DRUG SUBSTANCE (1)
10 DULOXETINE HYDROCHLORIDE USP (12)
11 DULOXETINE HYDROCHLORIDE USP (DUB ROUTE) (1)
12 DULOXETINE HYDROCHLORIDE USP (DUX PROCES) (1)
13 DULOXETINE HYDROCHLORIDE USP (NON-STERILE DRUG SUBSTANCE) (1)
14 DULOXETINE HYDROCHLORIDE USP (PROCESS B) (1)
15 DULOXETINE HYDROCHLORIDE USP (PROCESS II) (1)
16 DULOXETINE HYDROCHLORIDE USP (PROCESS-II) (1)
17 DULOXETINE HYDROCHLORIDE USP [ROUTE CODE - DX"] (1)
18 DULOXETINE HYDROCHLORIDE USP, NON-STERILE, BULK DRUG SUBSTANCE (1)
19 DULOXETINE HYDROCHLORIDE, NON-STERILE BULK DRUG SUBSTANCE (1)
20 DULOXETINE HYDROCHLORIDE, USP (2)
01 China (9)
02 India (27)
03 Israel (1)
04 Italy (2)
05 Mexico (1)
06 Spain (2)
07 Taiwan (2)
08 U.S.A (1)
01 Active (31)
02 Inactive (14)
01 Complete (16)
02 Blank (29)
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A Duloxetine HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duloxetine HCl, including repackagers and relabelers. The FDA regulates Duloxetine HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duloxetine HCl 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 Duloxetine HCl supplier is an individual or a company that provides Duloxetine HCl active pharmaceutical ingredient (API) or Duloxetine HCl finished formulations upon request. The Duloxetine HCl suppliers may include Duloxetine HCl API manufacturers, exporters, distributors and traders.
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A Duloxetine HCl DMF (Drug Master File) is a document detailing the whole manufacturing process of Duloxetine HCl active pharmaceutical ingredient (API) in detail. Different forms of Duloxetine HCl DMFs exist exist since differing nations have different regulations, such as Duloxetine HCl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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We have 37 companies offering Duloxetine HCl
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