Package 50090-7741-0

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-7741-0
Digits Only 5009077410
Product NDC 50090-7741
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7741-0)

Marketing

Marketing Status
Marketed Since 2025-10-29
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": "1ec63e68-97f0-4ebe-b6cf-a28fd8b9e693", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["ae1fc2e6-cc67-4b90-9e39-d1ec4e9d6773"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7741-0)", "package_ndc": "50090-7741-0", "marketing_start_date": "20251029"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "50090-7741_1ec63e68-97f0-4ebe-b6cf-a28fd8b9e693", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7741", "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": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}