| NDC Code | 69986-017-01 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69986-017-01) |
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| Product NDC | 69986-017 |
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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 | 20231222 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213612 |
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| Manufacturer | Sinotherapeutics Inc. |
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| Substance Name | PAROXETINE HYDROCHLORIDE HEMIHYDRATE |
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| Strength | 37.5 |
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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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