01 1Daito Co., Ltd.
02 1Kanto Chemical Co., Ltd.
01 1Carteolol hydrochloride salt
02 1Day stations carteolol hydrochloride (production only)
01 2Japan
Japanese Pharmacopoeia Carteolol Hydrochloride (for manufacturing purposes 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
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PharmaCompass offers a list of Carteolol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Carteolol manufacturer or Carteolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Carteolol manufacturer or Carteolol supplier.
A Cartrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cartrol, including repackagers and relabelers. The FDA regulates Cartrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cartrol 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 Cartrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cartrol supplier is an individual or a company that provides Cartrol active pharmaceutical ingredient (API) or Cartrol finished formulations upon request. The Cartrol suppliers may include Cartrol API manufacturers, exporters, distributors and traders.
click here to find a list of Cartrol suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Cartrol Drug Master File in Japan (Cartrol JDMF) empowers Cartrol 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 Cartrol JDMF during the approval evaluation for pharmaceutical products. At the time of Cartrol 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 Cartrol suppliers with JDMF on PharmaCompass.
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