Package 70518-0373-0

{"route": ["ORAL"], "spl_id": "47f52035-321a-3c7d-e063-6394a90a24ed", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C", "786Z46389E"], "rxcui": ["861740"], "spl_set_id": ["3f2599c6-9e33-487e-9379-6477bb121461"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0373-0)", "package_ndc": "70518-0373-0", "marketing_start_date": "20170403"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0373-1)", "package_ndc": "70518-0373-1", "marketing_start_date": "20170403"}], "brand_name": "Glipizide and Metformin Hydrochloride", "product_id": "70518-0373_47f52035-321a-3c7d-e063-6394a90a24ed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]", "Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-0373", "generic_name": "Glipizide and Metformin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide and Metformin Hydrochloride", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}, {"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077270", "marketing_category": "ANDA", "marketing_start_date": "20170403", "listing_expiration_date": "20271231"}