Package 68071-3723-3

{"route": ["ORAL"], "spl_id": "31e29202-2083-bc70-e063-6394a90afee8", "openfda": {"upc": ["0368071372335"], "unii": ["W5S57Y3A5L"], "rxcui": ["866924"], "spl_set_id": ["2760fbbc-ec68-4df8-e063-6394a90a15f5"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3723-3)", "package_ndc": "68071-3723-3", "marketing_start_date": "20241120"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-3723-6)", "package_ndc": "68071-3723-6", "marketing_start_date": "20241120"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68071-3723-8)", "package_ndc": "68071-3723-8", "marketing_start_date": "20241210"}], "brand_name": "Metoprolol Tartrate", "product_id": "68071-3723_31e29202-2083-bc70-e063-6394a90afee8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68071-3723", "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": "25 mg/1"}], "application_number": "ANDA200981", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}