Package 60760-566-90
Brand: metoprolol tartrate
Generic: metoprolol tartratePackage Facts
Identity
Package NDC
60760-566-90
Digits Only
6076056690
Product NDC
60760-566
Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-566-90)
Marketing
Marketing Status
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": "e55cd5cb-2279-a2c8-e053-2995a90a93af", "openfda": {"unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["e55cd5b5-c739-24ba-e053-2995a90a3ed4"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-566-90)", "package_ndc": "60760-566-90", "marketing_start_date": "20220727"}], "brand_name": "Metoprolol Tartrate", "product_id": "60760-566_e55cd5cb-2279-a2c8-e053-2995a90a93af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-566", "generic_name": "Metoprolol Tartrate", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20261231"}