01 1Esteve Quimica SA
02 1MSN Life Sciences Private Limited
03 1Pfizer Ireland Pharmaceuticals Unlimited Company
04 1SMS Pharmaceuticals Limited
01 1Nirmaltrelvir
02 2Nirmatrelvir
03 1nirmatrelvir
01 2India
02 1Spain
03 1Blank
NDC Package Code : 57572-0720
Start Marketing Date : 2022-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-105
Start Marketing Date : 2022-12-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67835-0034
Start Marketing Date : 2024-06-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60715-2085
Start Marketing Date : 2022-08-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Paxlovid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paxlovid, including repackagers and relabelers. The FDA regulates Paxlovid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paxlovid 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 Paxlovid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paxlovid supplier is an individual or a company that provides Paxlovid active pharmaceutical ingredient (API) or Paxlovid finished formulations upon request. The Paxlovid suppliers may include Paxlovid API manufacturers, exporters, distributors and traders.
click here to find a list of Paxlovid 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 Paxlovid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Paxlovid 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 Paxlovid 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 Paxlovid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Paxlovid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Paxlovid suppliers with NDC on PharmaCompass.
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