Package 72789-379-90

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 72789-379-90
Digits Only 7278937990
Product NDC 72789-379
Product ID 72789-379_2e810e95-939d-2ccd-e063-6394a90ab28e
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-379-90)

Marketing

Marketing Status
Marketed Since 2024-02-02
Brand paroxetine
Generic paroxetine hydrochloride hemihydrate
Sample Package No

Linked Drug Pages (1)

Paroxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2e810e95-939d-2ccd-e063-6394a90ab28e", "openfda": {"upc": ["0372789379906"], "unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["d551f3d0-9503-45bd-b701-dfed4c8a5e1e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-379-90)", "package_ndc": "72789-379-90", "marketing_start_date": "20240202"}], "brand_name": "Paroxetine", "product_id": "72789-379_2e810e95-939d-2ccd-e063-6394a90ab28e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72789-379", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20220329", "listing_expiration_date": "20261231"}