| NDC Code | 52959-812-22 |
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| Package Description | 22 TABLET in 1 BOTTLE (52959-812-22) |
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| Product NDC | 52959-812 |
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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 | 20031023 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040527 |
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| Manufacturer | H.J. Harkins Company, 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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