Package 60505-6151-1

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0432e6c3-ad77-726c-e063-6294a90a798c", "openfda": {"upc": ["0360505615216", "0360505615247", "0360505615148", "0360505614806", "0360505614844", "0360505614905"], "unii": ["023Z5BR09K"], "rxcui": ["309092", "1665005", "1665021", "1665046"], "spl_set_id": ["5116231f-82d1-44be-b08e-560c9a50e5c5"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (60505-6151-1)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "60505-6151-1", "marketing_start_date": "20170630"}, {"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (60505-6151-4)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "60505-6151-4", "marketing_start_date": "20170630"}], "brand_name": "Ceftriaxone Sodium", "product_id": "60505-6151_0432e6c3-ad77-726c-e063-6294a90a798c", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "60505-6151", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA203702", "marketing_category": "ANDA", "marketing_start_date": "20170630", "listing_expiration_date": "20261231"}