| NDC Code | 23155-174-03 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (23155-174-03) |
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| Product NDC | 23155-174 |
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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 Tablets |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20121019 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202061 |
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| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals 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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