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01 2M/s Emcure Pharmaceuticals Limited
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01 1Pentamidine Diisetionate Ph.Eur
02 1Pentamidine Isethionate USP
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01 2WC-0547
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01 2India
Pentamidine Diisetionate Ph.Eur
Date of Issue : 2022-12-30
Valid Till : 2025-12-30
Written Confirmation Number : WC-0547
Address of the Firm : Plot No. 12/2, F-II Block, M.I.D.C., Pimpri, Pune-411018, Taluka: Pimpri, Distri...
Date of Issue : 2022-12-30
Valid Till : 2025-12-30
Written Confirmation Number : WC-0547
Address of the Firm : Plot No. 12/2, F-II Block, M.I.D.C., Pimpri, Pune-411018, Taluka: Pimpri, Distri...
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PharmaCompass offers a list of Pentamidine Isethionate 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 Pentamidine Isethionate manufacturer or Pentamidine Isethionate supplier for your needs.
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PharmaCompass also assists you with knowing the Pentamidine Isethionate API Price utilized in the formulation of products. Pentamidine Isethionate API Price is not always fixed or binding as the Pentamidine Isethionate Price is obtained through a variety of data sources. The Pentamidine Isethionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NebuPent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NebuPent, including repackagers and relabelers. The FDA regulates NebuPent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NebuPent 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 NebuPent supplier is an individual or a company that provides NebuPent active pharmaceutical ingredient (API) or NebuPent finished formulations upon request. The NebuPent suppliers may include NebuPent API manufacturers, exporters, distributors and traders.
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A NebuPent written confirmation (NebuPent WC) is an official document issued by a regulatory agency to a NebuPent manufacturer, verifying that the manufacturing facility of a NebuPent active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting NebuPent APIs or NebuPent finished pharmaceutical products to another nation, regulatory agencies frequently require a NebuPent WC (written confirmation) as part of the regulatory process.
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