01 1M/s J P Laboratories Private Limited
01 1Isosorbide-5-Mononitrate IH
01 1WC-0106
01 1India
Date of Issue : 2022-12-30
Valid Till : 2025-07-26
Written Confirmation Number : WC-0106
Address of the Firm : A-76, MIDC, Kurkumbh, Daund, Pune-413801, Maharashtra, India
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PharmaCompass offers a list of Isosorbide Mononitrate 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 Isosorbide Mononitrate manufacturer or Isosorbide Mononitrate supplier for your needs.
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PharmaCompass also assists you with knowing the Isosorbide Mononitrate API Price utilized in the formulation of products. Isosorbide Mononitrate API Price is not always fixed or binding as the Isosorbide Mononitrate Price is obtained through a variety of data sources. The Isosorbide Mononitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Monomax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monomax, including repackagers and relabelers. The FDA regulates Monomax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monomax API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Monomax supplier is an individual or a company that provides Monomax active pharmaceutical ingredient (API) or Monomax finished formulations upon request. The Monomax suppliers may include Monomax API manufacturers, exporters, distributors and traders.
click here to find a list of Monomax suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Monomax written confirmation (Monomax WC) is an official document issued by a regulatory agency to a Monomax manufacturer, verifying that the manufacturing facility of a Monomax active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Monomax APIs or Monomax finished pharmaceutical products to another nation, regulatory agencies frequently require a Monomax WC (written confirmation) as part of the regulatory process.
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