| NDC Code | 54569-5912-2 |
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| Package Description | 90 TABLET in 1 BOTTLE (54569-5912-2) |
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| Product NDC | 54569-5912 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Benzphetamine Hydrochloride |
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| Non-Proprietary Name | Benzphetamine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20100721 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090968 |
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| Manufacturer | A-S Medication Solutions LLC |
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| Substance Name | BENZPHETAMINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC] |
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| DEA Schedule | CIII |
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