TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API India Private Limited
02 1Daito Co., Ltd.
03 1Glenmark Life Sciences Limited
04 1HANMI FINE CHEMICAL CO. , LTD.
05 1HANSEOCHEM CO. , LTD.
06 1Kongo Chemical Co., Ltd.
07 1MSN Laboratories Private Limited.
08 1Nantong Chanyoo Pharmatech Co. ,Ltd
09 1Sanyo Chemical Research Institute Co., Ltd.
10 2Tokuyama Corporation
11 1Zhejiang Tianyu Pharmaceutical Co. , Ltd.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 231MF10028
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2019-02-05
Latest Date of Registration : 2020-12-18
A Zetia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zetia, including repackagers and relabelers. The FDA regulates Zetia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zetia 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 Zetia manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zetia supplier is an individual or a company that provides Zetia active pharmaceutical ingredient (API) or Zetia finished formulations upon request. The Zetia suppliers may include Zetia API manufacturers, exporters, distributors and traders.
click here to find a list of Zetia 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 Zetia Drug Master File in Japan (Zetia JDMF) empowers Zetia 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 Zetia JDMF during the approval evaluation for pharmaceutical products. At the time of Zetia 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 Zetia suppliers with JDMF on PharmaCompass.
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