| NDC Code | 24090-722-88 |
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| Package Description | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (24090-722-88) |
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| Product NDC | 24090-722 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Suprenza |
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| Non-Proprietary Name | Phentermine Hydrochloride |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20121214 |
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| End Marketing Date | 20180930 |
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| Marketing Category Name | NDA |
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| Application Number | NDA202088 |
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| Manufacturer | Akrimax Pharmaceuticals, LLC |
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| Substance Name | PHENTERMINE HYDROCHLORIDE |
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| Strength | 37.5 |
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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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