| NDC Code: |
0555-0763 |
| Proprietary Name: |
Adderall |
| Suffix: |
|
| Non-Proprietary Name: |
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
11-08-2008 |
| Category Name: |
ANDA |
| Application Number: |
ANDA040422 |
| Labeler: |
BARR LABORATORIES INC. |
| Substance Name: |
AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE |
| Active Numerator Strength: |
1.875; 1.875; 1.875; 1.875 |
| Active Ingredient Unit: |
mg/1; mg/1; mg/1; mg/1 |
| Pharm 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] |
| DEA Schedule: |
CII |
