| NDC Code | 57664-641-08 |
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| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (57664-641-08) |
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| Product NDC | 57664-641 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, And Amphetamine Sulfate |
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| Non-Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, And Amphetamine Sulfate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20030909 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040480 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE |
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| Strength | 1.25; 1.25; 1.25; 1.25 |
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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 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], Central Nervous System Stimulation [PE] |
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| DEA Schedule | CII |
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