Package 68071-4880-1
Brand: metoprolol tartrate
Generic: metoprolol tartratePackage Facts
Identity
Package NDC
68071-4880-1
Digits Only
6807148801
Product NDC
68071-4880
Description
120 TABLET, FILM COATED in 1 BOTTLE (68071-4880-1)
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": "1ae1cc9d-0254-361f-e063-6394a90a966b", "openfda": {"upc": ["0368071488098"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["87ef9aa6-2faa-0f77-e053-2a95a90a3a26"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68071-4880-1)", "package_ndc": "68071-4880-1", "marketing_start_date": "20190502"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-4880-9)", "package_ndc": "68071-4880-9", "marketing_start_date": "20190502"}], "brand_name": "Metoprolol Tartrate", "product_id": "68071-4880_1ae1cc9d-0254-361f-e063-6394a90a966b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-4880", "generic_name": "Metoprolol Tartrate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20181201", "listing_expiration_date": "20261231"}