01 1Daiwa Pharmaceutical Industries Co., Ltd.
02 2Ipca Laboratories Limited
03 2KOLON LIFE SCIENCE, INC.
04 1Shin Poong Pharm. Co. , Ltd.
01 1Japanese Pharmacopoeia Drug zaltoprofen (production only)
02 4Zaltoprofen
03 1Zaltoprofen (N)
01 3India
02 3South Korea
Japanese Pharmacopoeia Drug Zaltoprofen (for manufacturing only)
Registration Number : 225MF10206
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2013-11-14
Latest Date of Registration : 2013-11-14
Registration Number : 227MF10154
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (West), Mumbai 400 067, India
Initial Date of Registration : 2015-06-01
Latest Date of Registration : 2018-10-12
Registration Number : 221MF10152
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (West), Mumbai 400 067, India
Initial Date of Registration : 2009-07-09
Latest Date of Registration : 2009-07-09
Registration Number : 218MF10020
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2007-03-23
Registration Number : 303MF10112
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2021-07-16
Latest Date of Registration : 2021-07-16
Registration Number : 304MF10156
Registrant's Address : 161, Yeoksam-ro, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2022-12-15
Latest Date of Registration : 2023-10-12
A Zaltoprofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zaltoprofen, including repackagers and relabelers. The FDA regulates Zaltoprofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zaltoprofen 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 Zaltoprofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zaltoprofen supplier is an individual or a company that provides Zaltoprofen active pharmaceutical ingredient (API) or Zaltoprofen finished formulations upon request. The Zaltoprofen suppliers may include Zaltoprofen API manufacturers, exporters, distributors and traders.
click here to find a list of Zaltoprofen 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 Zaltoprofen Drug Master File in Japan (Zaltoprofen JDMF) empowers Zaltoprofen 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 Zaltoprofen JDMF during the approval evaluation for pharmaceutical products. At the time of Zaltoprofen 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 Zaltoprofen suppliers with JDMF on PharmaCompass.
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