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 : 2025-12-31
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 : 2025-12-31
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 : 0406-1950
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 : 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 : 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
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PharmaCompass offers a list of Amphetamine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Amphetamine manufacturer or Amphetamine supplier for your needs.
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A ADDERALL XR 30-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ADDERALL XR 30-1, including repackagers and relabelers. The FDA regulates ADDERALL XR 30-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ADDERALL XR 30-1 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ADDERALL XR 30-1 supplier is an individual or a company that provides ADDERALL XR 30-1 active pharmaceutical ingredient (API) or ADDERALL XR 30-1 finished formulations upon request. The ADDERALL XR 30-1 suppliers may include ADDERALL XR 30-1 API manufacturers, exporters, distributors and traders.
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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 ADDERALL XR 30-1 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ADDERALL XR 30-1 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 ADDERALL XR 30-1 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 ADDERALL XR 30-1 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ADDERALL XR 30-1 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ADDERALL XR 30-1 suppliers with NDC on PharmaCompass.
We have 6 companies offering ADDERALL XR 30-1
Get in contact with the supplier of your choice:
