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 Plazilin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Plazilin, including repackagers and relabelers. The FDA regulates Plazilin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Plazilin 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 Plazilin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Plazilin supplier is an individual or a company that provides Plazilin active pharmaceutical ingredient (API) or Plazilin finished formulations upon request. The Plazilin suppliers may include Plazilin API manufacturers, exporters, distributors and traders.
click here to find a list of Plazilin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Plazilin written confirmation (Plazilin WC) is an official document issued by a regulatory agency to a Plazilin manufacturer, verifying that the manufacturing facility of a Plazilin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Plazilin APIs or Plazilin finished pharmaceutical products to another nation, regulatory agencies frequently require a Plazilin WC (written confirmation) as part of the regulatory process.
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