Package 68001-617-79

{"route": ["INTRAVENOUS"], "spl_id": "2094e27c-5df6-5cb8-e063-6294a90ae690", "openfda": {"nui": ["N0000000236", "N0000175558"], "upc": ["0368001617796", "0368001616775", "0368001615365"], "unii": ["50SG953SK6"], "rxcui": ["1740894", "1740898", "1740900"], "spl_set_id": ["57129df7-d6b1-419e-90ec-54f9b5182e7c"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (68001-617-79)  / 80 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-617-79", "marketing_start_date": "20240711"}], "brand_name": "MITOMYCIN", "product_id": "68001-617_2094e27c-5df6-5cb8-e063-6294a90ae690", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "68001-617", "generic_name": "MITOMYCIN", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MITOMYCIN", "active_ingredients": [{"name": "MITOMYCIN", "strength": "40 mg/80mL"}], "application_number": "ANDA216732", "marketing_category": "ANDA", "marketing_start_date": "20240711", "listing_expiration_date": "20261231"}