Package 72789-420-90

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 72789-420-90
Digits Only 7278942090
Product NDC 72789-420
Product ID 72789-420_2e822eda-69a5-addb-e063-6394a90a13b3
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-420-90)

Marketing

Marketing Status
Marketed Since 2024-07-12
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": "2e822eda-69a5-addb-e063-6394a90a13b3", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738511"], "spl_set_id": ["65c81817-34d3-4c57-a4bf-fb10be98386d"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-420-90)", "package_ndc": "72789-420-90", "marketing_start_date": "20240712"}], "brand_name": "Paroxetine", "product_id": "72789-420_2e822eda-69a5-addb-e063-6394a90a13b3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72789-420", "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": "40 mg/1"}], "application_number": "ANDA203854", "marketing_category": "ANDA", "marketing_start_date": "20220329", "listing_expiration_date": "20261231"}