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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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PharmaCompass offers a list of Duloxetine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Duloxetine manufacturer or Duloxetine supplier for your needs.
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PharmaCompass also assists you with knowing the Duloxetine API Price utilized in the formulation of products. Duloxetine API Price is not always fixed or binding as the Duloxetine Price is obtained through a variety of data sources. The Duloxetine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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.
We have 37 companies offering Duloxetine
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