| NDC Code | 60687-520-25 |
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-520-25) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-520-95) |
| Product NDC | 60687-520 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate |
| Non-Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate |
| Dosage Form | CAPSULE, EXTENDED RELEASE |
| Usage | ORAL |
| Start Marketing Date | 20200710 |
| End Marketing Date | 20230731 |
| Marketing Category Name | ANDA |
| Application Number | ANDA206159 |
| Manufacturer | American Health Packaging |
| Substance Name | AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE |
| Strength | 7.5; 7.5; 7.5; 7.5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmacy Classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Central Nervous System Stimulation [PE], Central Nervous System Stimulation [PE] |
| DEA Schedule | CII |