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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 Ajanta Pharma Limited (1)
03 Alembic Pharmaceuticals Limited (2)
04 Alkem Laboratories (1)
05 Aurobindo Pharma Limited (2)
06 CTX Lifesciences (1)
07 Cadila Pharmaceuticals (1)
08 Chongqing Shenghuaxi Pharma. Co., Ltd (1)
09 Erregierre SpA (1)
10 Esteve Quimica (1)
11 HEC Pharm (1)
12 Hansoh Pharma (1)
13 Hetero Drugs (1)
14 Jubilant Generics (1)
15 Lupin Ltd (2)
16 MATRIX LABORATORIES XIAMEN LTD. (1)
17 MSN Laboratories (2)
18 Macleods Pharmaceuticals Limited (2)
19 Nosch Labs Pvt. Ltd. (1)
20 Olon S.p.A (1)
21 Orchid Pharma (1)
22 R L Fine Chem (1)
23 RANBAXY LABORATORIES LIMITED (1)
24 SCI PHARMTECH (2)
25 Shanghai Wonder Pharmaceutical (1)
26 Shodhana Laboratories Pvt. Ltd (1)
27 Signa S.A. de C.V. (1)
28 Sun Pharmaceutical Industries Limited (1)
29 Teva API (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 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 supplier is an individual or a company that provides Cymbalta active pharmaceutical ingredient (API) or Cymbalta finished formulations upon request. The Cymbalta suppliers may include Cymbalta API manufacturers, exporters, distributors and traders.
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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.
A Cymbalta DMF submitted to regulatory agencies in the US is known as a USDMF. Cymbalta USDMF includes data on Cymbalta's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cymbalta USDMF is kept confidential to protect the manufacturer’s intellectual property.
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