01 1NARD Chemicals Inc.
02 2Neova Technologies, Inc.
03 1Nisshin Pharma Co., Ltd.
04 1Ouchi Shinko Chemical Industry Co., Ltd.
05 1Sankyo Kasei Co., Ltd.
06 1The Protein Company S. A.
07 1UBE Inc.
01 1Hydrochloric acid aprindine (production only)
02 1Hydrochloric acid arotinolol (production only)
03 1Hydrochloric acid bevantolol - Ube
04 1Hydrochloric acid selected from indisetron "Nissin"
05 1Japanese Pharmacopoeia lysozyme hydrochloride
06 1Lysozyme chloride
07 1Lysozyme chloride (CA)
08 1Outsiders regulations hydrochloric acid Benekisato Betadekusu (production only)
01 2Canada
02 5Japan
03 1Spain
Aprindine hydrochloride (for manufacturing purposes only)
Registration Number : 218MF10389
Registrant's Address : 2-6-1 Nishinagasucho, Amagasaki City, Hyogo Prefecture
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2018-04-09
Japanese Pharmacopoeia Lysozyme Hydrochloride
Registration Number : 219MF10145
Registrant's Address : 31212 Peardonville Road Abbottsford, BC Canada
Initial Date of Registration : 2007-04-27
Latest Date of Registration : 2007-04-27
Registration Number : 218MF10688
Registrant's Address : 31212 Peardonville Road Abbottsford, BC Canada
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
Indisetron hydrochloride "Nissin"
Registration Number : 217MF11112
Registrant's Address : 25 Kanda Nishikicho 1-chome, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-12-05
Latest Date of Registration : 2009-10-29
Arotinolol hydrochloride (for manufacturing only)
Registration Number : 217MF10695
Registrant's Address : 7-4, Nihonbashi Kofunecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2008-04-11
Registration Number : 218MF10284
Registrant's Address : Industrial Area 1, La Fagned'Hi Street 43-B6600 BASTOGNE, Belgium
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2009-11-24
Extra-official regulations Benexate hydrochloride Betadex (for manufacturing only)
Registration Number : 218MF10135
Registrant's Address : Osaka Prefecture, Osaka City, Kita Ward, Dojimahama 1-4-16
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2010-01-07
Bevantolol hydrochloride - Ube
Registration Number : 217MF10443
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-08-19
Latest Date of Registration : 2008-01-10
A Hydrochloric Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrochloric Acid, including repackagers and relabelers. The FDA regulates Hydrochloric Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrochloric Acid 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 Hydrochloric Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrochloric Acid supplier is an individual or a company that provides Hydrochloric Acid active pharmaceutical ingredient (API) or Hydrochloric Acid finished formulations upon request. The Hydrochloric Acid suppliers may include Hydrochloric Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrochloric Acid 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 Hydrochloric Acid Drug Master File in Japan (Hydrochloric Acid JDMF) empowers Hydrochloric Acid 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 Hydrochloric Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Hydrochloric Acid 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 Hydrochloric Acid suppliers with JDMF on PharmaCompass.
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