| NDC Code | 62542-030-30 | 
|---|
			| Package Description | 30 BLISTER PACK in 1 CARTON (62542-030-30)  / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 
|---|
			| Product NDC | 62542-030 | 
|---|
			| 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 | 18.8 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE] | 
|---|
			| DEA Schedule | CII | 
|---|