Package 45802-211-72

{"route": ["ORAL"], "spl_id": "187b18ba-520f-45dd-9d6f-57a833962da1", "openfda": {"upc": ["0345802169723", "0345802211729"], "unii": ["EEN99869SC", "786Z46389E"], "rxcui": ["1368385", "1368392"], "spl_set_id": ["14d98490-4f8f-4d2f-a4e9-7a3d7a0199ba"], "manufacturer_name": ["Padagis Israel Pharmaceuticals Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (45802-211-72)", "package_ndc": "45802-211-72", "marketing_start_date": "20160408"}], "brand_name": "alogliptin and metformin hydrochloride", "product_id": "45802-211_187b18ba-520f-45dd-9d6f-57a833962da1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "45802-211", "generic_name": "alogliptin and metformin hydrochloride", "labeler_name": "Padagis Israel Pharmaceuticals Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "alogliptin and metformin hydrochloride", "active_ingredients": [{"name": "ALOGLIPTIN BENZOATE", "strength": "12.5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "NDA203414", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160408", "listing_expiration_date": "20261231"}