| NDC Code | 62542-020-30 |
|---|
| Package Description | 30 BLISTER PACK in 1 CARTON (62542-020-30) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
|---|
| Product NDC | 62542-020 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amphetamine Extended-release |
|---|
| Non-Proprietary Name | Amphetamine Extended-release |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250901 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA204326 |
|---|
| Manufacturer | Neos Therapeutics, LP |
|---|
| Substance Name | AMPHETAMINE |
|---|
| Strength | 12.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE] |
|---|
| DEA Schedule | CII |
|---|