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