Package 68462-726-90

{"route": ["ORAL"], "spl_id": "4d1a25c6-4ffc-4714-98a9-c4dcb2049d6d", "openfda": {"unii": ["Z8J84YIX6L"], "rxcui": ["858036", "858042"], "spl_set_id": ["e286ffd4-c598-47fb-af06-2e15f7e6f99f"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68462-726-05)", "package_ndc": "68462-726-05", "marketing_start_date": "20230731"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68462-726-30)", "package_ndc": "68462-726-30", "marketing_start_date": "20230731"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68462-726-90)", "package_ndc": "68462-726-90", "marketing_start_date": "20230731"}], "brand_name": "SAXAGLIPTIN", "product_id": "68462-726_4d1a25c6-4ffc-4714-98a9-c4dcb2049d6d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Dipeptidyl Peptidase 4 Inhibitor [EPC]", "Dipeptidyl Peptidase 4 Inhibitors [MoA]"], "product_ndc": "68462-726", "generic_name": "SAXAGLIPTIN", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SAXAGLIPTIN", "active_ingredients": [{"name": "SAXAGLIPTIN HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA205994", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20271231"}