Package 0409-3365-10

{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "a3ebafac-648e-47b1-a6f5-1e3bff1e3e08", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897653", "897753", "897756", "897757", "897758", "1724276", "1724383", "1724644"], "spl_set_id": ["e9c9ef18-7dfc-4322-b2fc-29b934c30f8b"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0409-3365-10)  / 1 mL in 1 VIAL, SINGLE-DOSE (0409-3365-11)", "package_ndc": "0409-3365-10", "marketing_start_date": "20210614"}], "brand_name": "Hydromorphone Hydrochloride", "product_id": "0409-3365_a3ebafac-648e-47b1-a6f5-1e3bff1e3e08", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0409-3365", "dea_schedule": "CII", "generic_name": "HYDROMORPHONE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydromorphone Hydrochloride", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "NDA200403", "marketing_category": "NDA", "marketing_start_date": "20111201", "listing_expiration_date": "20261231"}