01 1Active Pharma Co., Ltd.
02 1CADILA PHARMACEUTICALS LIMITED.
03 1Garonit Pharmaceutical, Inc.
04 5Maruishi Pharmaceutical Co., Ltd.
01 1Chlorhexidine Gluconate
02 2Chlorhexidine gluconate Sanshioeki
03 1Chlorhexidine gluconate Sanshioeki (production only)
04 2Chlorhexidine gluconate solution
05 1Japanese Pharmacopoeia chlorhexidine gluconate Sanshioeki (production only)
06 1Japanese Pharmacopoeia chlorhexidine gluconate solution (production only)
01 1India
02 6Japan
03 1U.S.A
Chlorhexidine Gluconate Solution (for manufacturing purposes only)
Registration Number : 218MF10908
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
Chlorhexidine gluconate solution 20%
Registration Number : 305MF10128
Registrant's Address : 10 AB Madison Road, Fairfield NJ 07004 USA
Initial Date of Registration : 2023-12-06
Latest Date of Registration : 2023-12-06
Japanese Pharmacopoeia Chlorhexidine Gluconate Solution (for manufacturing purposes only)
Registration Number : 221MF10075
Registrant's Address : 2-4-2 Imazu-naka, Tsurumi-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2009-04-14
Latest Date of Registration : 2009-04-14
Chlorhexidine gluconate solution
Registration Number : 219MF10320
Registrant's Address : 2-4-2 Imazu-naka, Tsurumi-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2007-10-24
Latest Date of Registration : 2007-10-24
Chlorhexidine gluconate solution
Registration Number : 219MF10319
Registrant's Address : 2-4-2 Imazu-naka, Tsurumi-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2007-10-24
Latest Date of Registration : 2007-10-24
Chlorhexidine gluconate solution
Registration Number : 218MF10347
Registrant's Address : 2-3-5 Fushimi-cho, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2006-03-17
Chlorhexidine gluconate solution
Registration Number : 218MF10346
Registrant's Address : 2-3-5 Fushimi-cho, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2006-03-17
Japanese Pharmacopoeia Chlorhexidine Gluconate Solution (for manufacturing purposes only)
Registration Number : 217MF10192
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-08
Latest Date of Registration : 2022-09-14
53
PharmaCompass offers a list of Chlorhexidine Gluconate 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 Gluconate manufacturer or Chlorhexidine Gluconate supplier for your needs.
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PharmaCompass also assists you with knowing the Chlorhexidine Gluconate API Price utilized in the formulation of products. Chlorhexidine Gluconate API Price is not always fixed or binding as the Chlorhexidine Gluconate Price is obtained through a variety of data sources. The Chlorhexidine Gluconate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A pHiso-Med manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of pHiso-Med, including repackagers and relabelers. The FDA regulates pHiso-Med manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. pHiso-Med 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 pHiso-Med manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A pHiso-Med supplier is an individual or a company that provides pHiso-Med active pharmaceutical ingredient (API) or pHiso-Med finished formulations upon request. The pHiso-Med suppliers may include pHiso-Med API manufacturers, exporters, distributors and traders.
click here to find a list of pHiso-Med 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 pHiso-Med Drug Master File in Japan (pHiso-Med JDMF) empowers pHiso-Med 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 pHiso-Med JDMF during the approval evaluation for pharmaceutical products. At the time of pHiso-Med 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 pHiso-Med suppliers with JDMF on PharmaCompass.
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