| NDC Code | 68071-4315-9 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4315-9) |
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| Product NDC | 68071-4315 |
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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 | 20151120 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205528 |
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| Manufacturer | NuCare Pharmaceuticals,Inc. |
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| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
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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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