Package 0143-9245-10

{"route": ["INTRAVENOUS"], "spl_id": "bbbf119e-26f4-46c1-ba80-de927e51c566", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["7GR28W0FJI"], "rxcui": ["1731338"], "spl_set_id": ["0d81315c-7021-4091-b703-ad135390c936"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9245-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9245-01)", "package_ndc": "0143-9245-10", "marketing_start_date": "20010808"}], "brand_name": "Dacarbazine", "product_id": "0143-9245_bbbf119e-26f4-46c1-ba80-de927e51c566", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "0143-9245", "generic_name": "Dacarbazine", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dacarbazine", "active_ingredients": [{"name": "DACARBAZINE", "strength": "200 mg/1"}], "application_number": "ANDA075812", "marketing_category": "ANDA", "marketing_start_date": "20010808", "listing_expiration_date": "20261231"}