Package 60842-002-02

Brand: naloxone hydrochloride injection, usp, auto-injector

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60842-002-02
Digits Only 6084200202
Product NDC 60842-002
Product ID 60842-002_04afe7f9-83ba-4269-a6ce-3bcc61a106d8
Description

10 DOSE PACK in 1 CARTON (60842-002-02) / .4 mL in 1 DOSE PACK

Marketing

Marketing Status
Marketed Since 2022-02-28
Brand naloxone hydrochloride injection, usp, auto-injector
Generic naloxone hydrochloride
Sample Package No

Linked Drug Pages (1)

Naloxone Hydrochloride Injection, USP, Auto-Injector ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "SUBCUTANEOUS"], "spl_id": "04afe7f9-83ba-4269-a6ce-3bcc61a106d8", "openfda": {"unii": ["F850569PQR"], "rxcui": ["2596175"], "spl_set_id": ["b5463553-b775-47a3-8d10-31e01ca1ec72"], "manufacturer_name": ["Kaleo, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 DOSE PACK in 1 CARTON (60842-002-02)  / .4 mL in 1 DOSE PACK", "package_ndc": "60842-002-02", "marketing_start_date": "20220228"}], "brand_name": "Naloxone Hydrochloride Injection, USP, Auto-Injector", "product_id": "60842-002_04afe7f9-83ba-4269-a6ce-3bcc61a106d8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "60842-002", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Kaleo, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride Injection, USP, Auto-Injector", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "10 mg/.4mL"}], "application_number": "NDA215457", "marketing_category": "NDA", "marketing_start_date": "20220228", "listing_expiration_date": "20261231"}