Package 68475-001-50

{"route": ["INTRAVENOUS"], "spl_id": "e2b1772b-057e-4c1a-a3e1-6bbf7c2d770e", "openfda": {"upc": ["0368475001503"], "unii": ["OJ245FE5EU", "48N6U1781G"], "rxcui": ["984118"], "spl_set_id": ["fbc7bfe3-6faa-45a3-befb-9ad7963c0571"], "manufacturer_name": ["Navinta LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68475-001-50)  / 50 mL in 1 VIAL", "package_ndc": "68475-001-50", "marketing_start_date": "20210304"}], "brand_name": "Sodium Phenylacetate and sodium benzoate", "product_id": "68475-001_e2b1772b-057e-4c1a-a3e1-6bbf7c2d770e", "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": "68475-001", "generic_name": "Sodium Phenylacetate and sodium benzoate", "labeler_name": "Navinta LLC", "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": "ANDA205880", "marketing_category": "ANDA", "marketing_start_date": "20210304", "listing_expiration_date": "20261231"}