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.
12 1UBE Inc.
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
A Duloxetine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duloxetine Hydrochloride, including repackagers and relabelers. The FDA regulates Duloxetine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duloxetine Hydrochloride 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 Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duloxetine Hydrochloride supplier is an individual or a company that provides Duloxetine Hydrochloride active pharmaceutical ingredient (API) or Duloxetine Hydrochloride finished formulations upon request. The Duloxetine Hydrochloride suppliers may include Duloxetine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Duloxetine Hydrochloride 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 Duloxetine Hydrochloride Drug Master File in Japan (Duloxetine Hydrochloride JDMF) empowers Duloxetine Hydrochloride 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 Duloxetine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Duloxetine Hydrochloride 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 Duloxetine Hydrochloride suppliers with JDMF on PharmaCompass.
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