01 1Kothari Phytochemicals International
02 1Lusochimica S. p. A.
01 1CHLORPROPAMIDE
02 1Chlorpropamide
01 1India
02 1Italy
Registration Number : 225MF10148
Registrant's Address : Santhosh Raj Plaza 12/9, 2nd Floor Subbaraman Street Near Anna Bus Stand Ghandhi Naga...
Initial Date of Registration : 2013-07-25
Latest Date of Registration : 2013-07-25
Registration Number : 221MF10085
Registrant's Address : Via Libornese, 897 56122 La Vettola, Pisa
Initial Date of Registration : 2009-04-30
Latest Date of Registration : 2009-04-30
A Chlorpropamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorpropamide, including repackagers and relabelers. The FDA regulates Chlorpropamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorpropamide 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 Chlorpropamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorpropamide supplier is an individual or a company that provides Chlorpropamide active pharmaceutical ingredient (API) or Chlorpropamide finished formulations upon request. The Chlorpropamide suppliers may include Chlorpropamide API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorpropamide 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 Chlorpropamide Drug Master File in Japan (Chlorpropamide JDMF) empowers Chlorpropamide 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 Chlorpropamide JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorpropamide 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 Chlorpropamide suppliers with JDMF on PharmaCompass.
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