Package 0409-1467-01

{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "cbcbf107-67c0-4a8a-a25d-5a05c43a0bfd", "openfda": {"unii": ["ZU4275277R"], "rxcui": ["904415", "904440", "1866543", "1866551"], "spl_set_id": ["6025e8d4-5083-4c3a-58a0-050e7b0b6150"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 CARTON in 1 CASE (0409-1467-01)  / 1 VIAL, MULTI-DOSE in 1 CARTON (0409-1467-61)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0409-1467-01", "marketing_start_date": "20050516"}], "brand_name": "Nalbuphine Hydrochloride", "product_id": "0409-1467_cbcbf107-67c0-4a8a-a25d-5a05c43a0bfd", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "0409-1467", "generic_name": "NALBUPHINE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nalbuphine Hydrochloride", "active_ingredients": [{"name": "NALBUPHINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA070918", "marketing_category": "ANDA", "marketing_start_date": "20050516", "listing_expiration_date": "20261231"}