Package 82868-090-30

Brand: metoprolol tartrate

Generic: metoprolol
NDC Package

Package Facts

Identity

Package NDC 82868-090-30
Digits Only 8286809030
Product NDC 82868-090
Description

30 TABLET in 1 BOTTLE, PLASTIC (82868-090-30)

Marketing

Marketing Status
Marketed Since 2025-10-07
Brand metoprolol tartrate
Generic metoprolol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "471cc93d-6d30-bf85-e063-6294a90abc87", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["471ccbfe-96dd-7ab9-e063-6394a90a5bd6"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-090-30)", "package_ndc": "82868-090-30", "marketing_start_date": "20251007"}], "brand_name": "METOPROLOL TARTRATE", "product_id": "82868-090_471cc93d-6d30-bf85-e063-6294a90abc87", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82868-090", "generic_name": "METOPROLOL", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA202871", "marketing_category": "ANDA", "marketing_start_date": "20251007", "listing_expiration_date": "20261231"}