| NDC Code | 53002-2174-3 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (53002-2174-3) |
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| Product NDC | 53002-2174 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Paroxetine |
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| Non-Proprietary Name | Paroxetine Hydrochloride Hemihydrate |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20141101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203854 |
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| Manufacturer | RPK Pharmaceuticals, Inc. |
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| Substance Name | PAROXETINE HYDROCHLORIDE ANHYDROUS |
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| Strength | 20 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
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