| NDC Code | 68180-647-01 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-647-01) |
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| Product NDC | 68180-647 |
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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 |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20170306 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204134 |
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| Manufacturer | Lupin Pharmaceuticals, Inc. |
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| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
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| Strength | 12.5 |
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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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