Package 70518-4531-0

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 70518-4531-0
Digits Only 7051845310
Product NDC 70518-4531
Product ID 70518-4531_4522aa67-51d1-7d1c-e063-6294a90a6b5e
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4531-0)

Marketing

Marketing Status
Marketed Since 2025-12-04
Brand metoprolol succinate
Generic metoprolol succinate
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": "4522aa67-51d1-7d1c-e063-6294a90a6b5e", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427"], "spl_set_id": ["a34ba95a-a2d5-400e-8757-58c7bd20cad7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4531-0)", "package_ndc": "70518-4531-0", "marketing_start_date": "20251204"}], "brand_name": "Metoprolol Succinate", "product_id": "70518-4531_4522aa67-51d1-7d1c-e063-6294a90a6b5e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4531", "generic_name": "Metoprolol Succinate", "labeler_name": "REMEDYREPACK INC.", "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": "20251204", "listing_expiration_date": "20261231"}