| NDC Code | 71335-0049-7 |
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| Package Description | 21 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-7) |
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| Product NDC | 71335-0049 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diethylpropion Hydrochloride |
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| Proprietary Name Suffix | Er |
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| Non-Proprietary Name | Diethylpropion Hydrochloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20111024 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091680 |
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| Manufacturer | Bryant Ranch Prepack |
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| Substance Name | DIETHYLPROPION HYDROCHLORIDE |
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| Strength | 75 |
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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 | CIV |
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