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Moehs Group, a reference company in the production of pharmaceutical active ingredients. 
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01 MOEHS IBERICA, S. L. (1)
02 Assia Chemical Industries Ltd. (1)
03 ESTECHPHARMA CO. , LTD. (1)
04 Fuji Chemical Industry Co., Ltd. (1)
05 HANMI FINE CHEMICAL CO. , LTD. (1)
06 HETERO DRUGS LIMITED. (2)
07 INIST ST CO. , LTD. (1)
08 LUPIN LIMITED. (1)
09 MSN Laboratories Private Limited. (1)
10 Organic Synthetic Pharmaceutical Industry Co., Ltd. (1)
11 SCI Pharmtech, Inc. (1)
12 UBE Co., Ltd. (1)
01 Duloxetine Hydrochloride (8)
02 Duloxetine Hydrochloride (for manufacturing use only) (1)
03 Duloxetine hydrochloride (2)
04 Duloxetine hydrochloride "K" (1)
05 Duloxetine hydrochloride "Teva" (1)
01 India (4)
02 Israel (1)
03 Japan (3)
04 South Korea (3)
05 Spain (1)
06 Taiwan (1)
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Duloxetine manufacturer or Duloxetine supplier.
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 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.
click here to find a list of Cymbalta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
click here to find a list of Cymbalta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Cymbalta Drug Master File in Japan (Cymbalta JDMF) empowers Cymbalta API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Cymbalta JDMF during the approval evaluation for pharmaceutical products. At the time of Cymbalta JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Cymbalta suppliers with JDMF on PharmaCompass.
We have 12 companies offering Cymbalta
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