01 1MSN Laboratories Private Limited
02 1Unichem Laboratories Limited, India
03 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
01 1Prasugrel
02 1Prasugrel Base
03 1Prasugrel hydrochloride
01 1China
02 2India
NDC Package Code : 14501-0084
Start Marketing Date : 2013-09-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-048
Start Marketing Date : 2015-01-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64220-137
Start Marketing Date : 2011-02-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Prasugrel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prasugrel, including repackagers and relabelers. The FDA regulates Prasugrel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prasugrel 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 Prasugrel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prasugrel supplier is an individual or a company that provides Prasugrel active pharmaceutical ingredient (API) or Prasugrel finished formulations upon request. The Prasugrel suppliers may include Prasugrel API manufacturers, exporters, distributors and traders.
click here to find a list of Prasugrel 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 Prasugrel as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Prasugrel 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 Prasugrel 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 Prasugrel and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Prasugrel NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Prasugrel suppliers with NDC on PharmaCompass.
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