| NDC Code | 52959-329-21 |
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| Package Description | 21 TABLET, EXTENDED RELEASE in 1 VIAL (52959-329-21) |
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| Product NDC | 52959-329 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diethylpropion Hydrochloride |
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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 | 20170103 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091680 |
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| Manufacturer | H.J. Harkins Company, Inc. |
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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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