Package 70677-1283-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70677-1283-1
Digits Only 7067712831
Product NDC 70677-1283
Product ID 70677-1283_f2811e51-2239-492f-9e6e-bfe53668f877
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (70677-1283-1) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-04-01
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": ["NASAL"], "spl_id": "f2811e51-2239-492f-9e6e-bfe53668f877", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["577fbd57-7054-4536-86c1-d43bc99cc7b1"], "manufacturer_name": ["Strategic Sourcing Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (70677-1283-1)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70677-1283-1", "marketing_start_date": "20250401"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "70677-1283_f2811e51-2239-492f-9e6e-bfe53668f877", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "70677-1283", "generic_name": "naloxone hydrochloride", "labeler_name": "Strategic Sourcing Services 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": "20250401", "listing_expiration_date": "20261231"}