Package 50090-7591-0
Brand: metoprolol succinate
Generic: metoprolol succinatePackage 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
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"}