01 2CADILA PHARMACEUTICALS LIMITED.
02 1Dishman Biotech Limited
01 2Chlorhexidine
02 1Chlorhexidine to chlorine (production only)
01 3India
Chlorhexidine (for manufacturing only)
Registration Number : 225MF10217
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2013-12-03
Latest Date of Registration : 2013-12-03
Registration Number : 301MF10001
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2019-05-08
Latest Date of Registration : 2019-05-08
Registration Number : 225MF10194
Registrant's Address : 2nd floor, Bhadr-Raj Chambers, Swastik Cross Road, Navrangpura Ahmedabad 380 009 INDI...
Initial Date of Registration : 2013-10-23
Latest Date of Registration : 2013-10-23
A Chlorhexidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorhexidine, including repackagers and relabelers. The FDA regulates Chlorhexidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorhexidine 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 Chlorhexidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorhexidine supplier is an individual or a company that provides Chlorhexidine active pharmaceutical ingredient (API) or Chlorhexidine finished formulations upon request. The Chlorhexidine suppliers may include Chlorhexidine API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorhexidine 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 Chlorhexidine Drug Master File in Japan (Chlorhexidine JDMF) empowers Chlorhexidine 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 Chlorhexidine JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorhexidine 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 Chlorhexidine suppliers with JDMF on PharmaCompass.
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