Package 70511-101-50

{"route": ["INTRAVENOUS"], "spl_id": "c158c088-1ab5-4099-a174-96aba96feb11", "openfda": {"unii": ["OJ245FE5EU", "48N6U1781G"], "rxcui": ["984118"], "spl_set_id": ["3529be10-0004-4628-9ca1-67a8acd86b51"], "manufacturer_name": ["MAIA PHARMACEUTICALS, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70511-101-50)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70511-101-50", "marketing_start_date": "20170522"}], "brand_name": "SODIUM PHENYLACETATE AND SODIUM BENZOATE", "product_id": "70511-101_c158c088-1ab5-4099-a174-96aba96feb11", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Ammonium Ion Binding Activity [MoA]", "Ammonium Ion Binding Activity [MoA]", "Nitrogen Binding Agent [EPC]", "Nitrogen Binding Agent [EPC]"], "product_ndc": "70511-101", "generic_name": "sodium phenylacetate and sodium benzoate", "labeler_name": "MAIA PHARMACEUTICALS, INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM PHENYLACETATE AND SODIUM BENZOATE", "active_ingredients": [{"name": "SODIUM BENZOATE", "strength": "100 mg/mL"}, {"name": "SODIUM PHENYLACETATE", "strength": "100 mg/mL"}], "application_number": "ANDA208521", "marketing_category": "ANDA", "marketing_start_date": "20170522", "listing_expiration_date": "20261231"}