Package 72162-2376-2

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2376-2
Digits Only 7216223762
Product NDC 72162-2376
Product ID 72162-2376_fbe83ce1-e79c-417d-a2f2-432c96e6f1f1
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (72162-2376-2) / .1 mL in 1 VIAL, SINGLE-DOSE (72162-2376-4)

Marketing

Marketing Status
Marketed Since 2024-10-03
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": "fbe83ce1-e79c-417d-a2f2-432c96e6f1f1", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["ed549649-dcbd-41f7-a774-876906751c5a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (72162-2376-2)  / .1 mL in 1 VIAL, SINGLE-DOSE (72162-2376-4)", "package_ndc": "72162-2376-2", "marketing_start_date": "20241003"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "72162-2376_fbe83ce1-e79c-417d-a2f2-432c96e6f1f1", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "72162-2376", "generic_name": "naloxone hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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": "20230730", "listing_expiration_date": "20261231"}