Package 70436-203-80

{"route": ["INTRAVENOUS"], "spl_id": "49562559-8e19-fb8a-e063-6394a90a0966", "openfda": {"upc": ["0370436203802"], "unii": ["0WR771DJXV"], "rxcui": ["1812168"], "spl_set_id": ["ee09a55f-9992-48bb-b8d6-1184bd548536"], "manufacturer_name": ["Slate Run Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70436-203-80)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70436-203-80", "marketing_start_date": "20230403"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (70436-203-82)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70436-203-82", "marketing_start_date": "20230403"}], "brand_name": "Dobutamine", "product_id": "70436-203_49562559-8e19-fb8a-e063-6394a90a0966", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "70436-203", "generic_name": "dobutamine", "labeler_name": "Slate Run Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dobutamine", "active_ingredients": [{"name": "DOBUTAMINE HYDROCHLORIDE", "strength": "250 mg/20mL"}], "application_number": "ANDA216131", "marketing_category": "ANDA", "marketing_start_date": "20230403", "listing_expiration_date": "20271231"}