Package 0404-9923-01

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9923-01
Digits Only 0404992301
Product NDC 0404-9923
Product ID 0404-9923_fa27af58-0243-44f8-a3e5-a8e8f88f8d53
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9923-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Discontinued 2026-07-31
Brand naloxone hydrochloride
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

NALOXONE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "fa27af58-0243-44f8-a3e5-a8e8f88f8d53", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["10c22ce2-7dbe-4417-b8b4-602b190b1ddd"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9923-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9923-01", "marketing_end_date": "20260731", "marketing_start_date": "20220113"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "0404-9923_fa27af58-0243-44f8-a3e5-a8e8f88f8d53", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0404-9923", "generic_name": "naloxone hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA207633", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20220113"}