Package 50090-5060-0

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-5060-0
Digits Only 5009050600
Product NDC 50090-5060
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-5060-0)

Marketing

Marketing Status
Marketed Since 2020-05-26
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": "57110203-5ffb-4e13-a8f2-004a3336cf92", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["5b423eba-0a35-41b0-9338-fa4c6f5c6c7f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5060-0)", "package_ndc": "50090-5060-0", "marketing_start_date": "20200526"}], "brand_name": "Metoprolol Tartrate", "product_id": "50090-5060_57110203-5ffb-4e13-a8f2-004a3336cf92", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-5060", "generic_name": "Metoprolol Tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20271231"}