01 1M/s. Optimus Drugs (P) Limited
01 1Fenticonazole Nitrate (Ph.Eur)
01 1WC-0182
01 1India
Fenticonazole Nitrate (Ph.Eur)
Date of Issue : 2022-11-03
Valid Till : 2025-07-02
Written Confirmation Number : WC-0182
Address of the Firm : Sy.no. 239 and 240 Dothigudem Village, Pochampally mandal, Nalgonda, District-50...
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PharmaCompass also assists you with knowing the Fenticonazole Nitrate API Price utilized in the formulation of products. Fenticonazole Nitrate API Price is not always fixed or binding as the Fenticonazole Nitrate Price is obtained through a variety of data sources. The Fenticonazole Nitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Terlomexin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terlomexin, including repackagers and relabelers. The FDA regulates Terlomexin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terlomexin 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 Terlomexin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terlomexin supplier is an individual or a company that provides Terlomexin active pharmaceutical ingredient (API) or Terlomexin finished formulations upon request. The Terlomexin suppliers may include Terlomexin API manufacturers, exporters, distributors and traders.
click here to find a list of Terlomexin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Terlomexin written confirmation (Terlomexin WC) is an official document issued by a regulatory agency to a Terlomexin manufacturer, verifying that the manufacturing facility of a Terlomexin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Terlomexin APIs or Terlomexin finished pharmaceutical products to another nation, regulatory agencies frequently require a Terlomexin WC (written confirmation) as part of the regulatory process.
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