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01 1M/s. IPCA Laboratories Ltd.,
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01 1Metoclopramide Base (BP/JP/ Ph.Eur)
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01 1WC-0091
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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 Reliveran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Reliveran, including repackagers and relabelers. The FDA regulates Reliveran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Reliveran 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 Reliveran manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Reliveran supplier is an individual or a company that provides Reliveran active pharmaceutical ingredient (API) or Reliveran finished formulations upon request. The Reliveran suppliers may include Reliveran API manufacturers, exporters, distributors and traders.
click here to find a list of Reliveran suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Reliveran written confirmation (Reliveran WC) is an official document issued by a regulatory agency to a Reliveran manufacturer, verifying that the manufacturing facility of a Reliveran active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Reliveran APIs or Reliveran finished pharmaceutical products to another nation, regulatory agencies frequently require a Reliveran WC (written confirmation) as part of the regulatory process.
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