DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s. Dr. Reddy’s Laboratories Limited
01 1Lomustine (Ph. Eur.)
01 1WC-0039
01 1India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-06
Valid Till : 2025-07-07
Written Confirmation Number : WC-0039
Address of the Firm : Unit-I, Plot Nos.137, 138, 145 & 146, Sri Venkateswara Co- Operative Industrial ...
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PharmaCompass also assists you with knowing the Lomustine API Price utilized in the formulation of products. Lomustine API Price is not always fixed or binding as the Lomustine Price is obtained through a variety of data sources. The Lomustine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lomustina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lomustina, including repackagers and relabelers. The FDA regulates Lomustina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lomustina 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 Lomustina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lomustina supplier is an individual or a company that provides Lomustina active pharmaceutical ingredient (API) or Lomustina finished formulations upon request. The Lomustina suppliers may include Lomustina API manufacturers, exporters, distributors and traders.
click here to find a list of Lomustina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lomustina written confirmation (Lomustina WC) is an official document issued by a regulatory agency to a Lomustina manufacturer, verifying that the manufacturing facility of a Lomustina active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lomustina APIs or Lomustina finished pharmaceutical products to another nation, regulatory agencies frequently require a Lomustina WC (written confirmation) as part of the regulatory process.
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