Package 55150-328-10

{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "f8180672-ed74-4ac4-8ffc-0c51d2947765", "openfda": {"upc": ["0355150328017"], "unii": ["F850569PQR"], "rxcui": ["1191222"], "spl_set_id": ["2725b9c0-5b1e-498b-9ec5-ee76a62e656a"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (55150-328-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-328-10", "marketing_start_date": "20191104"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (55150-328-25)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-328-25", "marketing_start_date": "20191104"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "55150-328_f8180672-ed74-4ac4-8ffc-0c51d2947765", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "55150-328", "generic_name": "NALOXONE HYDROCHLORIDE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA212456", "marketing_category": "ANDA", "marketing_start_date": "20191104", "listing_expiration_date": "20261231"}