Package 70518-3680-1

Brand: metoprolol succinate

Generic: metoprolol succinate er tablets
NDC Package

Package Facts

Identity

Package NDC 70518-3680-1
Digits Only 7051836801
Product NDC 70518-3680
Product ID 70518-3680_45231836-5700-b6c5-e063-6394a90a915a
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3680-1)

Marketing

Marketing Status
Marketed Since 2025-12-04
Brand metoprolol succinate
Generic metoprolol succinate er tablets
Sample Package No

Linked Drug Pages (1)

Metoprolol Succinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45231836-5700-b6c5-e063-6394a90a915a", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866436"], "spl_set_id": ["28c22fb6-6cc9-4c41-b781-88b33b6c8cee"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3680-1)", "package_ndc": "70518-3680-1", "marketing_start_date": "20251204"}], "brand_name": "Metoprolol Succinate", "product_id": "70518-3680_45231836-5700-b6c5-e063-6394a90a915a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3680", "generic_name": "Metoprolol Succinate ER Tablets", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA211143", "marketing_category": "ANDA", "marketing_start_date": "20230313", "listing_expiration_date": "20261231"}