SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
01 1SCI Pharmtech, Inc.
02 1Procos S. p. A.
01 1Hydrochloric acid propafenone
02 1Propafenone Hydrochloride
01 1Italy
02 1Taiwan
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registration Number : 224MF10096
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2012-05-08
Latest Date of Registration : 2024-07-24
Registration Number : 217MF11295
Registrant's Address : Via Matteotti 249,28062 CAMERI(NOVARA)/ITALY
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2007-08-07
A Propafenone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propafenone, including repackagers and relabelers. The FDA regulates Propafenone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propafenone 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 Propafenone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Propafenone supplier is an individual or a company that provides Propafenone active pharmaceutical ingredient (API) or Propafenone finished formulations upon request. The Propafenone suppliers may include Propafenone API manufacturers, exporters, distributors and traders.
click here to find a list of Propafenone 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 Propafenone Drug Master File in Japan (Propafenone JDMF) empowers Propafenone 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 Propafenone JDMF during the approval evaluation for pharmaceutical products. At the time of Propafenone 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 Propafenone suppliers with JDMF on PharmaCompass.
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