Package 70882-132-60

Brand: metoprolol tartrate

Generic: metoprolol tartrate
NDC Package

Package Facts

Identity

Package NDC 70882-132-60
Digits Only 7088213260
Product NDC 70882-132
Description

60 TABLET, FILM COATED in 1 BOTTLE (70882-132-60)

Marketing

Marketing Status
Marketed Since 2007-09-11
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": "6478f769-c2cc-403a-ba3a-17fd73ac84c6", "openfda": {"upc": ["0370882133609", "0370882132602"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514", "866924"], "spl_set_id": ["e3a6e812-98ef-49bd-8319-c8fb9f46be06"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (70882-132-60)", "package_ndc": "70882-132-60", "marketing_start_date": "20070911"}], "brand_name": "Metoprolol Tartrate", "product_id": "70882-132_6478f769-c2cc-403a-ba3a-17fd73ac84c6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70882-132", "generic_name": "Metoprolol Tartrate", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "25 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}