Package 76420-596-10

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "045b6441-f12b-f2b4-e063-6394a90ad0ac", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665005"], "spl_set_id": ["f01cf0e5-caaf-4759-ba21-50f3aceff523"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (76420-596-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "76420-596-01", "marketing_start_date": "20230902"}, {"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (76420-596-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "76420-596-10", "marketing_start_date": "20230902"}], "brand_name": "Ceftriaxone Sodium", "product_id": "76420-596_045b6441-f12b-f2b4-e063-6394a90ad0ac", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "76420-596", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA203702", "marketing_category": "ANDA", "marketing_start_date": "20170630", "listing_expiration_date": "20261231"}