01 1Katsura Chemical Co., Ltd.
02 1Norbrook s. r. o.
01 2Procaine Hydrochloride
01 1Czech Republic
02 1Japan
Registration Number : 301MF10084
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2019-10-25
Latest Date of Registration : 2019-10-25
Registration Number : 222MF10079
Registrant's Address : c. p. 323, 533 54 Rybitvi, Czech Republic
Initial Date of Registration : 2010-03-09
Latest Date of Registration : 2010-03-09
A Procaine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Procaine, including repackagers and relabelers. The FDA regulates Procaine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Procaine 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 Procaine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Procaine supplier is an individual or a company that provides Procaine active pharmaceutical ingredient (API) or Procaine finished formulations upon request. The Procaine suppliers may include Procaine API manufacturers, exporters, distributors and traders.
click here to find a list of Procaine 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 Procaine Drug Master File in Japan (Procaine JDMF) empowers Procaine 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 Procaine JDMF during the approval evaluation for pharmaceutical products. At the time of Procaine 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 Procaine suppliers with JDMF on PharmaCompass.
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