Package 54288-124-10

{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "f0223f84-ddc4-45a8-94e8-22cd1a39f19e", "openfda": {"upc": ["0354288124010"], "unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["5de44ee7-6525-4857-9a67-8882e96dbeb5"], "manufacturer_name": ["BPI Labs LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 PACKAGE in 1 CARTON (54288-124-01)  / 2 mL in 1 PACKAGE", "package_ndc": "54288-124-01", "marketing_start_date": "20231115"}, {"sample": false, "description": "10 PACKAGE in 1 CARTON (54288-124-10)  / 2 mL in 1 PACKAGE", "package_ndc": "54288-124-10", "marketing_start_date": "20231115"}], "brand_name": "Naloxone Hydrochloride", "product_id": "54288-124_f0223f84-ddc4-45a8-94e8-22cd1a39f19e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "54288-124", "generic_name": "Naloxone Hydrochloride", "labeler_name": "BPI Labs LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA216977", "marketing_category": "ANDA", "marketing_start_date": "20231115", "listing_expiration_date": "20261231"}