Package 80425-0409-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80425-0409-1
Digits Only 8042504091
Product NDC 80425-0409
Product ID 80425-0409_1be2d8f6-f643-69a6-e063-6294a90a327f
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (80425-0409-1) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2024-06-27
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": ["NASAL"], "spl_id": "1be2d8f6-f643-69a6-e063-6294a90a327f", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["1be2e38b-55ca-abea-e063-6394a90ac548"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (80425-0409-1)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "80425-0409-1", "marketing_start_date": "20240627"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "80425-0409_1be2d8f6-f643-69a6-e063-6294a90a327f", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "80425-0409", "generic_name": "naloxone hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA211951", "marketing_category": "ANDA", "marketing_start_date": "20240627", "listing_expiration_date": "20261231"}