| NDC Code | 62542-020-31 |
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| Package Description | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62542-020-31) |
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| Product NDC | 62542-020 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amphetamine Extended-release |
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| Non-Proprietary Name | Amphetamine Extended-release |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20250901 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA204326 |
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| Manufacturer | Neos Therapeutics, LP |
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| Substance Name | AMPHETAMINE |
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| Strength | 12.5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE] |
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| DEA Schedule | CII |
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