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
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PharmaCompass offers a list of Chlorhexidine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Chlorhexidine manufacturer or Chlorhexidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorhexidine manufacturer or Chlorhexidine supplier.
PharmaCompass also assists you with knowing the Chlorhexidine API Price utilized in the formulation of products. Chlorhexidine API Price is not always fixed or binding as the Chlorhexidine Price is obtained through a variety of data sources. The Chlorhexidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Periochip manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Periochip, including repackagers and relabelers. The FDA regulates Periochip manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Periochip 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 Periochip manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Periochip supplier is an individual or a company that provides Periochip active pharmaceutical ingredient (API) or Periochip finished formulations upon request. The Periochip suppliers may include Periochip API manufacturers, exporters, distributors and traders.
click here to find a list of Periochip 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 Periochip Drug Master File in Japan (Periochip JDMF) empowers Periochip 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 Periochip JDMF during the approval evaluation for pharmaceutical products. At the time of Periochip 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 Periochip suppliers with JDMF on PharmaCompass.
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