| NDC Code | 0603-5192-32 |
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| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5192-32) |
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| Product NDC | 0603-5192 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phentermine Hydrochloride |
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| Non-Proprietary Name | Phentermine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20020104 |
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| End Marketing Date | 20170731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040377 |
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| Manufacturer | Qualitest Pharmaceuticals |
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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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