01 1Daito Co., Ltd.
02 1Kanto Chemical Co., Ltd.
01 1Carteolol hydrochloride salt
02 1Day stations carteolol hydrochloride (production only)
01 2Japan
JP Carteolol Hydrochloride (for manufacturing only)
Registration Number : 219MF10024
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-01-22
Latest Date of Registration : 2007-01-22
Registration Number : 221MF10036
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2009-02-09
Latest Date of Registration : 2009-02-09
A (+/-)-Carteolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+/-)-Carteolol Hydrochloride, including repackagers and relabelers. The FDA regulates (+/-)-Carteolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+/-)-Carteolol Hydrochloride 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 (+/-)-Carteolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+/-)-Carteolol Hydrochloride supplier is an individual or a company that provides (+/-)-Carteolol Hydrochloride active pharmaceutical ingredient (API) or (+/-)-Carteolol Hydrochloride finished formulations upon request. The (+/-)-Carteolol Hydrochloride suppliers may include (+/-)-Carteolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of (+/-)-Carteolol Hydrochloride 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 (+/-)-Carteolol Hydrochloride Drug Master File in Japan ((+/-)-Carteolol Hydrochloride JDMF) empowers (+/-)-Carteolol Hydrochloride 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 (+/-)-Carteolol Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of (+/-)-Carteolol Hydrochloride 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 (+/-)-Carteolol Hydrochloride suppliers with JDMF on PharmaCompass.
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