Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1MOEHS IBERICA, S. L.
02 1SCI Pharmtech, Inc.
03 1Assia Chemical Industries Ltd.
04 1Fuji Chemical Industry Co., Ltd.
05 1HANMI FINE CHEMICAL CO. , LTD.
06 2HETERO DRUGS LIMITED.
07 1INIST ST CO. , LTD.
08 1LUPIN LIMITED.
09 1MSN Laboratories Private Limited.
10 1Organic Synthesis Chemicals Co., Ltd.
11 1Polaris AI Pharma Corp.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 302MF10013
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2020-01-27
Latest Date of Registration : 2020-01-27
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registration Number : 229MF10017
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2017-01-25
Latest Date of Registration : 2017-01-25
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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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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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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).
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