Package 50090-7363-0

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-7363-0
Digits Only 5009073630
Product NDC 50090-7363
Product ID 50090-7363_c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7363-0)

Marketing

Marketing Status
Marketed Since 2024-10-18
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Metoprolol Tartrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["771c262d-e1db-4a75-9609-110c27c43e51"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7363-0)", "package_ndc": "50090-7363-0", "marketing_start_date": "20241018"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-7363_c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7363", "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": "25 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}