Package 42708-041-60

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-041-60
Digits Only 4270804160
Product NDC 42708-041
Description

60 TABLET, FILM COATED in 1 BOTTLE (42708-041-60)

Marketing

Marketing Status
Marketed Since 2018-03-30
Brand metoprolol tartrate
Generic metoprolol tartrate
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b3f0b5-aff2-8f42-e063-6394a90a0203", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["2ad0606c-7a90-44bd-a75d-d256de30fbcf"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "60 TABLET, FILM COATED in 1 BOTTLE (42708-041-60)", "package_ndc": "42708-041-60", "marketing_start_date": "20180330"}], "brand_name": "Metoprolol Tartrate", "product_id": "42708-041_45b3f0b5-aff2-8f42-e063-6394a90a0203", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42708-041", "generic_name": "Metoprolol Tartrate", "labeler_name": "QPharma Inc", "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": "20261231"}