Package 72789-535-90

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 72789-535-90
Digits Only 7278953590
Product NDC 72789-535
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-535-90)

Marketing

Marketing Status
Marketed Since 2025-11-19
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4838ae05-6c01-774b-e063-6394a90a55b8", "openfda": {"upc": ["0372789535906"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["d3628f24-8076-4980-a358-8445ef8260f4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-535-90)", "package_ndc": "72789-535-90", "marketing_start_date": "20251119"}], "brand_name": "Metoprolol Tartrate", "product_id": "72789-535_4838ae05-6c01-774b-e063-6394a90a55b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72789-535", "generic_name": "Metoprolol Tartrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20271231"}