| NDC Code | 11534-160-03 |
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| Package Description | 1000 TABLET in 1 BOTTLE (11534-160-03) |
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| Product NDC | 11534-160 |
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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 | 20170124 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205008 |
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| Manufacturer | SUNRISE PHARMACEUTICAL, 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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