Veranova: A CDMO that manages complexity with confidence.
01 2Veranova, L.P.
02 5Cambrex Charles City, Inc
03 2Chattem Chemicals, Inc.
04 2Curia New York, Inc.
05 2Siegfried USA, LLC
06 2SpecGx LLC
01 1(S)-Alpha-Methylphenethylamine Sulphate
02 1AMPHETAMINE SULFATE
03 4Amphetamine Sulfate
04 4Dextroamphetamine Sulfate
05 2Phenyl-2-(R,S)-Aminopropane Sulfate
06 2Phenyl-2-(S)-Aminopropane Sulfate
07 1dextroamphetamine sulfate
01 2Ireland
02 2Switzerland
03 11U.S.A
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0058
Start Marketing Date : 1999-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0059
Start Marketing Date : 1999-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-1940
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-1941
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-1942
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-1970
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-4942
Start Marketing Date : 2013-11-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-1950
Start Marketing Date : 2013-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-3936
Start Marketing Date : 2022-12-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0792-3939
Start Marketing Date : 2023-11-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Amphetamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amphetamine, including repackagers and relabelers. The FDA regulates Amphetamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amphetamine 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 Amphetamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amphetamine supplier is an individual or a company that provides Amphetamine active pharmaceutical ingredient (API) or Amphetamine finished formulations upon request. The Amphetamine suppliers may include Amphetamine API manufacturers, exporters, distributors and traders.
click here to find a list of Amphetamine 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 Amphetamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Amphetamine 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 Amphetamine 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 Amphetamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Amphetamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Amphetamine suppliers with NDC on PharmaCompass.
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