Package 0404-9767-10

{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCONJUNCTIVAL"], "spl_id": "f07091d0-6f67-4cd7-8fae-3cce4b3385af", "openfda": {"unii": ["ZU4275277R"], "rxcui": ["904415"], "spl_set_id": ["4ef2c0dc-3ab4-4bb1-aff0-523e3c23ad2d"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (0404-9767-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0404-9767-10", "marketing_start_date": "20251211"}], "brand_name": "Nalbuphine Hydrochloride", "product_id": "0404-9767_f07091d0-6f67-4cd7-8fae-3cce4b3385af", "dosage_form": "INJECTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "0404-9767", "generic_name": "nalbuphine hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nalbuphine Hydrochloride", "active_ingredients": [{"name": "NALBUPHINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA216049", "marketing_category": "ANDA", "marketing_start_date": "20251211", "listing_expiration_date": "20261231"}