Package 42708-147-60

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package Sample

Package Facts

Identity

Package NDC 42708-147-60
Digits Only 4270814760
Product NDC 42708-147
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-147-60)

Marketing

Marketing Status
Marketed Since 2021-04-23
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": "4586b1ca-b20b-f78a-e063-6394a90a2523", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["c0e147a8-36a6-1e61-e053-2a95a90afd62"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-147-60)", "package_ndc": "42708-147-60", "marketing_start_date": "20210423"}], "brand_name": "Metoprolol Tartrate", "product_id": "42708-147_4586b1ca-b20b-f78a-e063-6394a90a2523", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "42708-147", "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"}