Package 76420-867-02

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-867-02
Digits Only 7642086702
Product NDC 76420-867
Product ID 76420-867_259ab241-9f39-0383-e063-6394a90a040c
Description

2 BLISTER PACK in 1 CARTON (76420-867-02) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2024-10-29
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": "259ab241-9f39-0383-e063-6394a90a040c", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["7acf3bde-f858-4fbc-8a11-6741a3d27b8e"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (76420-867-02)  / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "76420-867-02", "marketing_start_date": "20241029"}], "brand_name": "Naloxone Hydrochloride", "product_id": "76420-867_259ab241-9f39-0383-e063-6394a90a040c", "dosage_form": "SPRAY, METERED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "76420-867", "generic_name": "Naloxone Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naloxone Hydrochloride", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA209522", "marketing_category": "ANDA", "marketing_start_date": "20240923", "listing_expiration_date": "20261231"}