Package 82804-165-90

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 82804-165-90
Digits Only 8280416590
Product NDC 82804-165
Description

90 TABLET, FILM COATED in 1 BOTTLE (82804-165-90)

Marketing

Marketing Status
Marketed Since 2024-12-16
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c43fe89-2283-482e-9d97-648d3ed183f8", "openfda": {"upc": ["0382804165902"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["3c43fe89-2283-482e-9d97-648d3ed183f8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-165-90)", "package_ndc": "82804-165-90", "marketing_start_date": "20241216"}], "brand_name": "Metoprolol Tartrate", "product_id": "82804-165_3c43fe89-2283-482e-9d97-648d3ed183f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82804-165", "generic_name": "Metoprolol Tartrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}