| NDC Code | 51079-825-62 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 DOSE PACK (51079-825-62) |
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| Product NDC | 51079-825 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Paroxetine Hydrochloride |
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| Non-Proprietary Name | Paroxetine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20120912 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077873 |
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| Manufacturer | Mylan Institutional Inc. |
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| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
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| Strength | 25 |
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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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