Package 71288-814-81

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71288-814-81
Digits Only 7128881481
Product NDC 71288-814
Product ID 71288-814_56d28c41-a00f-46f3-9c13-c62c20954555
Description

10 SYRINGE in 1 CARTON (71288-814-81) / 1 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2026-01-01
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": "56d28c41-a00f-46f3-9c13-c62c20954555", "openfda": {"unii": ["F850569PQR"], "rxcui": ["2679504"], "spl_set_id": ["c2daaefa-6c24-4e91-9176-61e9713069fa"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (71288-814-81)  / 1 mL in 1 SYRINGE", "package_ndc": "71288-814-81", "marketing_start_date": "20260101"}], "brand_name": "Naloxone Hydrochloride", "product_id": "71288-814_56d28c41-a00f-46f3-9c13-c62c20954555", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "71288-814", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".4 mg/mL"}], "application_number": "ANDA214211", "marketing_category": "ANDA", "marketing_start_date": "20260101", "listing_expiration_date": "20261231"}