01 1Harman Finochem Ltd.
01 1Succinylcholine Chloride
01 1India
Registration Number : 304MF10080
Registrant's Address : 107-A, Vinay Bhavya Complex, 159-A, C. S. T Road, Kalina, Santa Cruz (East), Mumbai-4...
Initial Date of Registration : 2022-05-25
Latest Date of Registration : 2022-05-25
A Suxamethonium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Suxamethonium Chloride, including repackagers and relabelers. The FDA regulates Suxamethonium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Suxamethonium Chloride 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 Suxamethonium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Suxamethonium Chloride supplier is an individual or a company that provides Suxamethonium Chloride active pharmaceutical ingredient (API) or Suxamethonium Chloride finished formulations upon request. The Suxamethonium Chloride suppliers may include Suxamethonium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Suxamethonium Chloride 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 Suxamethonium Chloride Drug Master File in Japan (Suxamethonium Chloride JDMF) empowers Suxamethonium Chloride 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 Suxamethonium Chloride JDMF during the approval evaluation for pharmaceutical products. At the time of Suxamethonium Chloride 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 Suxamethonium Chloride suppliers with JDMF on PharmaCompass.
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