Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech Co. , Ltd.
02 1TAPI Hungary Industries Ltd.
03 2Biocon Limited
04 2Guangdong Blue Treasure Pharmaceuticals Co. , Ltd.
05 1Kyowa Hakko Bio Co., Ltd.
06 2Shanghai Tianwei Biopharmaceutical Co., Ltd.
01 1Day stations
02 1Japanese Pharmacopoeia pravastatin sodium (production only)
03 1Pravastatin Sodium
04 1Pravastatin lactone (intermediate)
05 4Pravastatin sodium
06 1Pravastatin sodium "Teva"
01 4China
02 2India
03 1Israel
04 1Japan
05 1Taiwan
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 218MF10474
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2006-04-27
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 218MF10727
Registrant's Address : 13 Pallagi u(´)t, Debrecen, 4042-Hungary
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2015-12-15
Registration Number : 223MF10039
Registrant's Address : 20th K. M. Hosur Road, Electronics City-560100, Bangalore, India
Initial Date of Registration : 2011-03-10
Latest Date of Registration : 2011-03-10
Registration Number : 223MF10038
Registrant's Address : 20th KM Hosur Road, Electronics City, Bengaluru-560 100, Karnataka, India.
Initial Date of Registration : 2011-03-10
Latest Date of Registration : 2018-03-30
Registration Number : 231MF10011
Registrant's Address : No. 44, Renmin One Road, Qingyuan, Guangdong Province, P. R. China
Initial Date of Registration : 2019-01-10
Latest Date of Registration : 2019-01-10
Pravastatin lactone (intermediate)
Registration Number : 306MF10030
Registrant's Address : No. 44, Renmin One Road, Qingyuan, Guangdong Province, P. R. China
Initial Date of Registration : 2024-02-21
Latest Date of Registration : 2024-02-21
Japanese Pharmacopoeia Pravastatin Sodium (for manufacturing only)
Registration Number : 219MF10201
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2007-06-13
Latest Date of Registration : 2007-06-13
Registration Number : 229MF10176
Registrant's Address : No. 4258 Jindu Road, Shanghai, China
Initial Date of Registration : 2017-09-07
Latest Date of Registration : 2017-09-07
Registration Number : 219MF10113
Registrant's Address : No. 4258 Jindu Road, Shanghai, China
Initial Date of Registration : 2007-03-23
Latest Date of Registration : 2014-04-02
A Pravastatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pravastatin, including repackagers and relabelers. The FDA regulates Pravastatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pravastatin 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 Pravastatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pravastatin supplier is an individual or a company that provides Pravastatin active pharmaceutical ingredient (API) or Pravastatin finished formulations upon request. The Pravastatin suppliers may include Pravastatin API manufacturers, exporters, distributors and traders.
click here to find a list of Pravastatin 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 Pravastatin Drug Master File in Japan (Pravastatin JDMF) empowers Pravastatin 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 Pravastatin JDMF during the approval evaluation for pharmaceutical products. At the time of Pravastatin 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 Pravastatin suppliers with JDMF on PharmaCompass.
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