Package 70518-4533-0

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 70518-4533-0
Digits Only 7051845330
Product NDC 70518-4533
Product ID 70518-4533_4585bc02-0106-e4d3-e063-6394a90aa88d
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4533-0)

Marketing

Marketing Status
Marketed Since 2025-12-09
Brand metoprolol succinate
Generic metoprolol succinate
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4585bc02-0106-e4d3-e063-6394a90aa88d", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412"], "spl_set_id": ["a46cbf09-20e3-4f0d-ab41-221f60fde068"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4533-0)", "package_ndc": "70518-4533-0", "marketing_start_date": "20251209"}], "brand_name": "Metoprolol Succinate", "product_id": "70518-4533_4585bc02-0106-e4d3-e063-6394a90aa88d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4533", "generic_name": "Metoprolol Succinate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20251209", "listing_expiration_date": "20261231"}