Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
01 1EGIS PHARMACEUTICALS PRIVATE LIMITED COMPANY
02 1Shanghai Med-Pharma Factory Fifteen Co. Ltd.
01 1Chlorpromazine Hydrochloride
02 1Chlorpromazine hydrochloride
01 1Hungary
02 1Blank
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Registration Number : 304MF10157
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2022-12-15
Latest Date of Registration : 2022-12-15
Registration Number : 219MF10261
Registrant's Address : 1440 Bei Di Road. Shanghai, China
Initial Date of Registration : 2007-08-06
Latest Date of Registration : 2007-08-06
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PharmaCompass offers a list of Chlorpromazine Hydrochloride 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 Chlorpromazine Hydrochloride manufacturer or Chlorpromazine Hydrochloride supplier for your needs.
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A Megaphen hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Megaphen hydrochloride, including repackagers and relabelers. The FDA regulates Megaphen hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Megaphen 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 Megaphen hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Megaphen hydrochloride supplier is an individual or a company that provides Megaphen hydrochloride active pharmaceutical ingredient (API) or Megaphen hydrochloride finished formulations upon request. The Megaphen hydrochloride suppliers may include Megaphen hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Megaphen hydrochloride 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 Megaphen hydrochloride Drug Master File in Japan (Megaphen hydrochloride JDMF) empowers Megaphen 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 Megaphen hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Megaphen 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 Megaphen hydrochloride suppliers with JDMF on PharmaCompass.
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