| NDC Code | 60687-221-32 |
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| Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-221-32) > 1 CAPSULE in 1 BLISTER PACK (60687-221-33) |
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| Product NDC | 60687-221 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate |
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| Non-Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, And Amphetamine Sulfate |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20170103 |
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| End Marketing Date | 20180531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076852 |
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| Manufacturer | American Health Packaging |
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| Substance Name | DEXTROAMPHETAMINE SACCHARATE; AMPHETAMINE ASPARTATE MONOHYDRATE; DEXTROAMPHETAMINE SULFATE; AMPHETAMINE SULFATE |
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| Strength | 7.5; 7.5; 7.5; 7.5 |
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| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
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| Pharmacy 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] |
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| DEA Schedule | CII |
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