Package 63629-9321-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-9321-1
Digits Only 6362993211
Product NDC 63629-9321
Product ID 63629-9321_2b9592cc-ed48-4703-a8d2-85f0a8792d19
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (63629-9321-1) / .1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-07-07
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": "2b9592cc-ed48-4703-a8d2-85f0a8792d19", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["73edcc70-d988-4f66-a09a-8d23042283c3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (63629-9321-1)  / .1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63629-9321-1", "marketing_start_date": "20220707"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "63629-9321_2b9592cc-ed48-4703-a8d2-85f0a8792d19", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "63629-9321", "generic_name": "naloxone hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "4 mg/.1mL"}], "application_number": "ANDA211951", "marketing_category": "ANDA", "marketing_start_date": "20220621", "listing_expiration_date": "20261231"}