Package 72266-236-01

{"route": ["INTRAVENOUS"], "spl_id": "18084634-4c12-58ee-e063-6294a90ac7d3", "openfda": {"unii": ["OJ245FE5EU", "48N6U1781G"], "rxcui": ["2560228"], "spl_set_id": ["cee1e9a2-bbe5-2419-e053-2a95a90ac3ef"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72266-236-01)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72266-236-01", "marketing_start_date": "20211114"}], "brand_name": "Sodium Phenylacetate and Sodium Benzoate", "product_id": "72266-236_18084634-4c12-58ee-e063-6294a90ac7d3", "dosage_form": "INJECTION", "pharm_class": ["Ammonium Ion Binding Activity [MoA]", "Ammonium Ion Binding Activity [MoA]", "Nitrogen Binding Agent [EPC]", "Nitrogen Binding Agent [EPC]"], "product_ndc": "72266-236", "generic_name": "Sodium Phenylacetate and Sodium Benzoate", "labeler_name": "FOSUN PHARMA USA 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": "NDA215025", "marketing_category": "NDA", "marketing_start_date": "20211114", "listing_expiration_date": "20261231"}