| NDC Code | 68382-670-05 |
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| Package Description | 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-670-05) |
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| Product NDC | 68382-670 |
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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, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20180208 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204663 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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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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