Package 70756-658-10

{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "bc5568c5-97d3-49b1-94c7-f9f3c6c9d409", "openfda": {"upc": ["0370756658825", "0370756658108", "0370756658252"], "unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["ef647e2a-84e7-4e3e-942a-b6fc250141b6"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-10)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70756-658-10", "marketing_start_date": "20240229"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-25)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70756-658-25", "marketing_start_date": "20240229"}, {"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-82)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70756-658-82", "marketing_start_date": "20240229"}], "brand_name": "naloxone hydrochloride", "product_id": "70756-658_bc5568c5-97d3-49b1-94c7-f9f3c6c9d409", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "70756-658", "generic_name": "naloxone hydrochloride", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "naloxone hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA218404", "marketing_category": "ANDA", "marketing_start_date": "20240229", "listing_expiration_date": "20261231"}