Adderall - 63629-3768-1 - (Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate)

Alphabetical Index


Drug Information of Adderall

Product NDC: 63629-3768
Proprietary Name: Adderall
Non Proprietary Name: Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate
Active Ingredient(s): 2.5; 2.5; 2.5; 2.5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Adderall

Product NDC: 63629-3768
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040422
Marketing Category: ANDA
Start Marketing Date: 19960213

Package Information of Adderall

Package NDC: 63629-3768-1
Package Description: 30 TABLET in 1 BOTTLE (63629-3768-1)

NDC Information of Adderall

NDC Code 63629-3768-1
Proprietary Name Adderall
Package Description 30 TABLET in 1 BOTTLE (63629-3768-1)
Product NDC 63629-3768
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960213
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Strength Number 2.5; 2.5; 2.5; 2.5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Adderall


General Information