Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Rexim (Nanning) Pharmaceutical Co. , Ltd.
02 1Ajinomoto do Brazil Industria e Comercio de Alimentos Ltda.
03 1Kamiishiwabasa Acid Co., Ltd.
04 1Kyowa Hakko Bio Co., Ltd.
05 1SHINE STAR (HUBEI) BIOLOGICAL ENGINEERING CO. , LTD.
06 1Shanghai Ajinomoto Amino Acid Co., Ltd.
07 1Taenaka Mining Co., Ltd.
01 4Japanese Pharmacopoeia L- isoleucine (production only)
02 1Japanese Pharmacopoeia L-isoleucine (manufacturing only)
03 1L- isoleucine L-Isoleucine
04 1L-Isoleucine
01 1China
02 1Germany
03 4Japan
04 1Blank
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
Registration Number : 218MF10978
Registrant's Address : No. 10 Wenjiang Road, Wuming District, Nanning, 530100, Guangxi, P. R. China
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2011-11-07
Japanese Pharmacopoeia L-Isoleucine (for manufacturing only)
Registration Number : 219MF10243
Registrant's Address : Avenida Oriento, s/n Bairro Entre Rios-CEP 18500-000, Laranjal Paulista, SP, Brazil
Initial Date of Registration : 2007-07-17
Latest Date of Registration : 2007-07-17
Japanese Pharmacopoeia L-Isoleucine (for manufacturing only)
Registration Number : 226MF10084
Registrant's Address : No. 718, Rongle East Road, Songjiang District, Shanghai, People's Republic of China
Initial Date of Registration : 2014-05-09
Latest Date of Registration : 2014-05-09
Japanese Pharmacopoeia L-Isoleucine (for manufacturing only)
Registration Number : 217MF10221
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2006-11-15
Registration Number : 305MF10063
Registrant's Address : No. 666 Chanling Avenue, Douhudi Town, Gong An, Jingzhou, Hubei, P. R. China
Initial Date of Registration : 2023-05-17
Latest Date of Registration : 2023-05-17
Japanese Pharmacopoeia L-Isoleucine (for manufacturing only)
Registration Number : 217MF10288
Registrant's Address : 452 Oshiba, Mobara City, Chiba Prefecture
Initial Date of Registration : 2005-06-20
Latest Date of Registration : 2009-12-03
Japanese Pharmacopoeia L-Isoleucine (for manufacturing only)
Registration Number : 229MF10079
Registrant's Address : No. 158, Xinduan Road, Gongyuan District, Qingpu, Shanghai City, China
Initial Date of Registration : 2017-04-11
Latest Date of Registration : 2017-04-11
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PharmaCompass offers a list of Isoleucine 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 Isoleucine manufacturer or Isoleucine supplier for your needs.
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PharmaCompass also assists you with knowing the Isoleucine API Price utilized in the formulation of products. Isoleucine API Price is not always fixed or binding as the Isoleucine Price is obtained through a variety of data sources. The Isoleucine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 04Y7590D77 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04Y7590D77, including repackagers and relabelers. The FDA regulates 04Y7590D77 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04Y7590D77 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 04Y7590D77 supplier is an individual or a company that provides 04Y7590D77 active pharmaceutical ingredient (API) or 04Y7590D77 finished formulations upon request. The 04Y7590D77 suppliers may include 04Y7590D77 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 04Y7590D77 Drug Master File in Japan (04Y7590D77 JDMF) empowers 04Y7590D77 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 04Y7590D77 JDMF during the approval evaluation for pharmaceutical products. At the time of 04Y7590D77 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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