Package 0404-9773-01

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9773-01
Digits Only 0404977301
Product NDC 0404-9773
Product ID 0404-9773_dfa64508-45a2-41b2-b20f-eccda5e05c29
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9773-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-10-28
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": "dfa64508-45a2-41b2-b20f-eccda5e05c29", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["ddeebc32-9aab-4a2f-8c87-74335d17d5ef"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9773-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9773-01", "marketing_start_date": "20251028"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "0404-9773_dfa64508-45a2-41b2-b20f-eccda5e05c29", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "0404-9773", "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": "ANDA218404", "marketing_category": "ANDA", "marketing_start_date": "20251028", "listing_expiration_date": "20261231"}