Package 69547-627-02

Brand: narcan

Generic: naloxone hydrochloride nasal
NDC Package

Package Facts

Identity

Package NDC 69547-627-02
Digits Only 6954762702
Product NDC 69547-627
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (69547-627-02) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2023-08-28
Brand narcan
Generic naloxone hydrochloride nasal
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "eca68b75-c15c-4ee0-a352-a4ec66e57424", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059", "1725064"], "spl_set_id": ["a0ebc83d-2892-40de-bc0a-775ce90b30db"], "manufacturer_name": ["Emergent Devices Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (69547-627-02)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "69547-627-02", "marketing_start_date": "20230828"}], "brand_name": "NARCAN", "product_id": "69547-627_eca68b75-c15c-4ee0-a352-a4ec66e57424", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "69547-627", "generic_name": "naloxone hydrochloride nasal", "labeler_name": "Emergent Devices Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NARCAN", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "NDA208411", "marketing_category": "NDA", "marketing_start_date": "20230828", "listing_expiration_date": "20261231"}