Package 67457-292-02

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67457-292-02
Digits Only 6745729202
Product NDC 67457-292
Product ID 67457-292_292c264d-927b-43a6-b9eb-00154f5d13de
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (67457-292-02) / 1 mL in 1 VIAL, SINGLE-DOSE (67457-292-00)

Marketing

Marketing Status
Marketed Since 2014-03-06
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": "292c264d-927b-43a6-b9eb-00154f5d13de", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1659929"], "spl_set_id": ["f0932877-1f3b-4d5e-82d2-dd6c53db4730"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (67457-292-02)  / 1 mL in 1 VIAL, SINGLE-DOSE (67457-292-00)", "package_ndc": "67457-292-02", "marketing_start_date": "20140306"}], "brand_name": "Naloxone Hydrochloride", "product_id": "67457-292_292c264d-927b-43a6-b9eb-00154f5d13de", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "67457-292", "generic_name": "naloxone hydrochloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA204997", "marketing_category": "ANDA", "marketing_start_date": "20140306", "listing_expiration_date": "20261231"}