01 1DARMERICA, LLC
02 1MAEDA INC
01 1LOMUSTINE
02 1Lomustine
01 1U.S.A
02 1Blank
NDC Package Code : 71052-171
Start Marketing Date : 2020-05-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10g/10g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 86184-227
Start Marketing Date : 2023-07-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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Corporate PDF
A Lomustine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lomustine, including repackagers and relabelers. The FDA regulates Lomustine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lomustine 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 Lomustine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lomustine supplier is an individual or a company that provides Lomustine active pharmaceutical ingredient (API) or Lomustine finished formulations upon request. The Lomustine suppliers may include Lomustine API manufacturers, exporters, distributors and traders.
click here to find a list of Lomustine 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 Lomustine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lomustine 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 Lomustine 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 Lomustine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lomustine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lomustine suppliers with NDC on PharmaCompass.
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