Package 72189-652-90

Brand: metoprolol succinate er

Generic: metoprolol succinate er
NDC Package

Package Facts

Identity

Package NDC 72189-652-90
Digits Only 7218965290
Product NDC 72189-652
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-652-90)

Marketing

Marketing Status
Marketed Since 2025-12-08
Brand metoprolol succinate er
Generic metoprolol succinate er
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45723206-1a9e-5299-e063-6294a90ad969", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427"], "spl_set_id": ["45723206-1a9d-5299-e063-6294a90ad969"], "manufacturer_name": ["DIrect_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-652-90)", "package_ndc": "72189-652-90", "marketing_start_date": "20251208"}], "brand_name": "Metoprolol Succinate ER", "product_id": "72189-652_45723206-1a9e-5299-e063-6294a90ad969", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-652", "generic_name": "Metoprolol Succinate ER", "labeler_name": "DIrect_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Succinate ER", "active_ingredients": [{"name": "METOPROLOL SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA216916", "marketing_category": "ANDA", "marketing_start_date": "20251208", "listing_expiration_date": "20261231"}