Package 50090-7591-0

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 50090-7591-0
Digits Only 5009075910
Product NDC 50090-7591
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7591-0)

Marketing

Marketing Status
Marketed Since 2025-07-01
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef8226be-9604-4e38-8446-8589137a179d", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427"], "spl_set_id": ["4da96d34-ae8e-4c63-8ba0-bbeefdc20516"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7591-0)", "package_ndc": "50090-7591-0", "marketing_start_date": "20250701"}], "brand_name": "Metoprolol Succinate", "product_id": "50090-7591_ef8226be-9604-4e38-8446-8589137a179d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7591", "generic_name": "Metoprolol Succinate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20231002", "listing_expiration_date": "20261231"}