01 1RPG Life Sciences Limited
01 1Propantheline Bromide
01 1India
Registration Number : 303MF10144
Registrant's Address : RPG House, 463, Dr. Annie Besant Road, Worli, Mumbai 400030, India.
Initial Date of Registration : 2021-09-09
Latest Date of Registration : 2024-06-18
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PharmaCompass offers a list of Propantheline Bromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Propantheline Bromide manufacturer or Propantheline Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propantheline Bromide manufacturer or Propantheline Bromide supplier.
PharmaCompass also assists you with knowing the Propantheline Bromide API Price utilized in the formulation of products. Propantheline Bromide API Price is not always fixed or binding as the Propantheline Bromide Price is obtained through a variety of data sources. The Propantheline Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Propantel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propantel, including repackagers and relabelers. The FDA regulates Propantel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propantel 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 Propantel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Propantel supplier is an individual or a company that provides Propantel active pharmaceutical ingredient (API) or Propantel finished formulations upon request. The Propantel suppliers may include Propantel API manufacturers, exporters, distributors and traders.
click here to find a list of Propantel 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 Propantel Drug Master File in Japan (Propantel JDMF) empowers Propantel 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 Propantel JDMF during the approval evaluation for pharmaceutical products. At the time of Propantel 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 Propantel suppliers with JDMF on PharmaCompass.
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