Package 82868-087-90

Brand: metoprolol succinate

Generic: metoprolol succinate
NDC Package

Package Facts

Identity

Package NDC 82868-087-90
Digits Only 8286808790
Product NDC 82868-087
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-087-90)

Marketing

Marketing Status
Marketed Since 2025-09-15
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": "471f16b3-f7fd-35f3-e063-6394a90a09d1", "openfda": {"unii": ["TH25PD4CCB"], "rxcui": ["866427"], "spl_set_id": ["471f154c-197f-31df-e063-6394a90ae73e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-087-90)", "package_ndc": "82868-087-90", "marketing_start_date": "20250915"}], "brand_name": "Metoprolol Succinate", "product_id": "82868-087_471f16b3-f7fd-35f3-e063-6394a90a09d1", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82868-087", "generic_name": "Metoprolol Succinate", "labeler_name": "Northwind Health Company, LLC", "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": "20250915", "listing_expiration_date": "20261231"}