01 1Megafine Pharma (P) Limited
01 1Piranterupamo salt (production only)
01 1India
Pyrantel pamoate (for manufacturing purposes only)
Registration Number : 221MF10046
Registrant's Address : Sethna 4th floor 55 Maharshi karve road Marine Lines,Mumbai-400002,INDIA
Initial Date of Registration : 2009-02-25
Latest Date of Registration : 2018-10-12
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PharmaCompass offers a list of Pyrantel Pamoate 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 Pyrantel Pamoate manufacturer or Pyrantel Pamoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pyrantel Pamoate manufacturer or Pyrantel Pamoate supplier.
PharmaCompass also assists you with knowing the Pyrantel Pamoate API Price utilized in the formulation of products. Pyrantel Pamoate API Price is not always fixed or binding as the Pyrantel Pamoate Price is obtained through a variety of data sources. The Pyrantel Pamoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PYRANTEL PAMOATE USP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PYRANTEL PAMOATE USP, including repackagers and relabelers. The FDA regulates PYRANTEL PAMOATE USP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PYRANTEL PAMOATE USP 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 PYRANTEL PAMOATE USP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PYRANTEL PAMOATE USP supplier is an individual or a company that provides PYRANTEL PAMOATE USP active pharmaceutical ingredient (API) or PYRANTEL PAMOATE USP finished formulations upon request. The PYRANTEL PAMOATE USP suppliers may include PYRANTEL PAMOATE USP API manufacturers, exporters, distributors and traders.
click here to find a list of PYRANTEL PAMOATE USP 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 PYRANTEL PAMOATE USP Drug Master File in Japan (PYRANTEL PAMOATE USP JDMF) empowers PYRANTEL PAMOATE USP 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 PYRANTEL PAMOATE USP JDMF during the approval evaluation for pharmaceutical products. At the time of PYRANTEL PAMOATE USP 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 PYRANTEL PAMOATE USP suppliers with JDMF on PharmaCompass.
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