Package 70518-4407-0

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 70518-4407-0
Digits Only 7051844070
Product NDC 70518-4407
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4407-0)

Marketing

Marketing Status
Marketed Since 2025-07-28
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": "47e0bb75-5cdf-966f-e063-6394a90a51da", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866412"], "spl_set_id": ["874a38ba-667e-47b6-a918-a972c0e3ed59"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4407-0)", "package_ndc": "70518-4407-0", "marketing_start_date": "20250728"}], "brand_name": "Metoprolol succinate", "product_id": "70518-4407_47e0bb75-5cdf-966f-e063-6394a90a51da", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4407", "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": "ANDA213854", "marketing_category": "ANDA", "marketing_start_date": "20250728", "listing_expiration_date": "20271231"}