| NDC Code | 69367-335-30 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69367-335-30) |
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| Product NDC | 69367-335 |
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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 | 20210726 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213485 |
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| Manufacturer | Westminster Pharmaceuticals, LLC |
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| Substance Name | PAROXETINE HYDROCHLORIDE |
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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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