| NDC Code | 17224-672-30 |
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| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (17224-672-30) |
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| Product NDC | 17224-672 |
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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 | 20100101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090968 |
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| Manufacturer | Calvin Scott & Co., Inc. |
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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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