Axplora- The partner of choice for complex APIs.
01 1PharmaZell (India) Private Limited
02 2PharmaZell GmbH
03 2Zhejiang Hengkang Pharmaceutical Co. , Ltd.
04 1Bayer Pharma AG
05 1CHEMI S. p. A.
06 1Cadila Healthcare Limited
07 1Cambrex Karlskoga AB
08 1DIVI'S LABORATORIES LIMITED
09 2ERREGIERRE S. p. A.
10 1SUN PHARMACEUTICAL INDUSTRIES LTD.
Axplora- The partner of choice for complex APIs.
Registration Number : 219MF10036
Registrant's Address : ROSENHEIMER STR. 43 D-83064 RAUBLING, Germany
Initial Date of Registration : 2007-02-13
Latest Date of Registration : 2016-02-02
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Registration Number : 305MF10102
Registrant's Address : No. 11 Chengen Road, Pubagan Town, Sanmen, Zhejiang, China
Initial Date of Registration : 2023-08-30
Latest Date of Registration : 2023-08-30
Axplora- The partner of choice for complex APIs.
Registration Number : 226MF10019
Registrant's Address : ROSENHEIMER STR. 43 D-83064 RAUBLING, GERMARY
Initial Date of Registration : 2014-01-21
Latest Date of Registration : 2014-01-21
Axplora- The partner of choice for complex APIs.
Registration Number : 226MF10064
Registrant's Address : Plot No. 115, Visakha Pharmacity Limited, SEZ, Parawada, Anakapalli - 531 019, Andhra...
Initial Date of Registration : 2014-03-11
Latest Date of Registration : 2014-03-11
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Registration Number : 227MF10271
Registrant's Address : No. 1 Longxiang Road, Hairun Street, Sanmen, Zhejiang, China
Initial Date of Registration : 2015-12-01
Latest Date of Registration : 2015-12-01
A CAS-89-57-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-89-57-6, including repackagers and relabelers. The FDA regulates CAS-89-57-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-89-57-6 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 CAS-89-57-6 supplier is an individual or a company that provides CAS-89-57-6 active pharmaceutical ingredient (API) or CAS-89-57-6 finished formulations upon request. The CAS-89-57-6 suppliers may include CAS-89-57-6 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-89-57-6 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 CAS-89-57-6 Drug Master File in Japan (CAS-89-57-6 JDMF) empowers CAS-89-57-6 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 CAS-89-57-6 JDMF during the approval evaluation for pharmaceutical products. At the time of CAS-89-57-6 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 CAS-89-57-6 suppliers with JDMF on PharmaCompass.
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