Package 50090-7488-0

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-7488-0
Digits Only 5009074880
Product NDC 50090-7488
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7488-0)

Marketing

Marketing Status
Marketed Since 2024-12-23
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": "5cd403bd-4a96-4c5a-a4bc-20da0920b3d7", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["8739b5c6-36ce-435f-b006-be8216c1c3dc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7488-0)", "package_ndc": "50090-7488-0", "marketing_start_date": "20241223"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-7488_5cd403bd-4a96-4c5a-a4bc-20da0920b3d7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7488", "generic_name": "Metoprolol Tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}