Package 0404-9766-10

Brand: nalbuphine hydrochloride

Generic: nalbuphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9766-10
Digits Only 0404976610
Product NDC 0404-9766
Description

1 VIAL, MULTI-DOSE in 1 BAG (0404-9766-10) / 10 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2025-12-10
Brand nalbuphine hydrochloride
Generic nalbuphine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "6aba69e2-1158-445c-87fc-b56b7391a9b3", "openfda": {"unii": ["ZU4275277R"], "rxcui": ["904440"], "spl_set_id": ["dd621bfa-ce48-4c27-b247-a6d885f70b72"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (0404-9766-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0404-9766-10", "marketing_start_date": "20251210"}], "brand_name": "Nalbuphine Hydrochloride", "product_id": "0404-9766_6aba69e2-1158-445c-87fc-b56b7391a9b3", "dosage_form": "INJECTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "0404-9766", "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": "20 mg/mL"}], "application_number": "ANDA216049", "marketing_category": "ANDA", "marketing_start_date": "20251210", "listing_expiration_date": "20261231"}