01 1M/s. IPCA Laboratories Ltd.,
01 1Metoclopramide Base (BP/JP/ Ph.Eur)
01 1WC-0091
01 1India
Metoclopramide Base (BP/JP/ Ph.Eur)
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091
Address of the Firm : Sejavta, Ratlam, Madhya Pradesh
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PharmaCompass offers a list of Metoclopramide 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 Metoclopramide manufacturer or Metoclopramide supplier for your needs.
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PharmaCompass also assists you with knowing the Metoclopramide API Price utilized in the formulation of products. Metoclopramide API Price is not always fixed or binding as the Metoclopramide Price is obtained through a variety of data sources. The Metoclopramide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pramin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pramin, including repackagers and relabelers. The FDA regulates Pramin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pramin 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 Pramin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pramin supplier is an individual or a company that provides Pramin active pharmaceutical ingredient (API) or Pramin finished formulations upon request. The Pramin suppliers may include Pramin API manufacturers, exporters, distributors and traders.
click here to find a list of Pramin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pramin written confirmation (Pramin WC) is an official document issued by a regulatory agency to a Pramin manufacturer, verifying that the manufacturing facility of a Pramin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pramin APIs or Pramin finished pharmaceutical products to another nation, regulatory agencies frequently require a Pramin WC (written confirmation) as part of the regulatory process.
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