01 1RPG Life Sciences Limited
02 1Tokuyama Corporation
01 1Japanese Pharmacopoeia propantheline bromide (production only)
02 1Propantheline Bromide
01 1India
02 1Japan
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
Japanese Pharmacopoeia Propantheline Bromide (For manufacturing purposes only)
Registration Number : 221MF10068
Registrant's Address : 1-1 Mikage-cho, Shunan City, Yamaguchi Prefecture
Initial Date of Registration : 2009-03-26
Latest Date of Registration : 2009-03-26
46
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 DSSTox_CID_3519 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3519, including repackagers and relabelers. The FDA regulates DSSTox_CID_3519 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3519 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 DSSTox_CID_3519 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DSSTox_CID_3519 supplier is an individual or a company that provides DSSTox_CID_3519 active pharmaceutical ingredient (API) or DSSTox_CID_3519 finished formulations upon request. The DSSTox_CID_3519 suppliers may include DSSTox_CID_3519 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_3519 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 DSSTox_CID_3519 Drug Master File in Japan (DSSTox_CID_3519 JDMF) empowers DSSTox_CID_3519 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 DSSTox_CID_3519 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_CID_3519 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 DSSTox_CID_3519 suppliers with JDMF on PharmaCompass.
We have 2 companies offering DSSTox_CID_3519
Get in contact with the supplier of your choice:
