01 1M/s JP Laboratories
02 1M/s. J. P. Laboratories Pvt. Ltd.,
01 1Isosorbide-5-Mononitrate IH
02 1Isosorbide-5-Mononitrate
01 1WC-0106
02 1WC0106
01 2India
Date of Issue : 2019-07-26
Valid Till : 2022-07-26
Written Confirmation Number : WC-0106
Address of the Firm : A-76, Cleareing Zone, MIDC, Kurkumbh, Daund-413 801, Dist Pune
Date of Issue : 2019-07-26
Valid Till : 2022-07-25
Written Confirmation Number : WC0106
Address of the Firm : A-76,MIDC, Chemical Zone, Kurkumbh, Tal, Daund, Pune
26
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 Uniket manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uniket, including repackagers and relabelers. The FDA regulates Uniket manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uniket 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 Uniket supplier is an individual or a company that provides Uniket active pharmaceutical ingredient (API) or Uniket finished formulations upon request. The Uniket suppliers may include Uniket API manufacturers, exporters, distributors and traders.
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A Uniket written confirmation (Uniket WC) is an official document issued by a regulatory agency to a Uniket manufacturer, verifying that the manufacturing facility of a Uniket active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Uniket APIs or Uniket finished pharmaceutical products to another nation, regulatory agencies frequently require a Uniket WC (written confirmation) as part of the regulatory process.
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