DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
01 1Pemetrexed Ditromethamine Dihydrate
01 1India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-970
Start Marketing Date : 2014-06-24
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Pemetrexed Ditromethamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pemetrexed Ditromethamine, including repackagers and relabelers. The FDA regulates Pemetrexed Ditromethamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pemetrexed Ditromethamine 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 Pemetrexed Ditromethamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pemetrexed Ditromethamine supplier is an individual or a company that provides Pemetrexed Ditromethamine active pharmaceutical ingredient (API) or Pemetrexed Ditromethamine finished formulations upon request. The Pemetrexed Ditromethamine suppliers may include Pemetrexed Ditromethamine API manufacturers, exporters, distributors and traders.
click here to find a list of Pemetrexed Ditromethamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Pemetrexed Ditromethamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pemetrexed Ditromethamine API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Pemetrexed Ditromethamine as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Pemetrexed Ditromethamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pemetrexed Ditromethamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pemetrexed Ditromethamine suppliers with NDC on PharmaCompass.
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