Package 51662-1659-2

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1659-2
Digits Only 5166216592
Product NDC 51662-1659
Product ID 51662-1659_19b0603b-2420-f439-e063-6294a90ae85f
Description

2 VIAL, SINGLE-DOSE in 1 CARTON (51662-1659-2) / .1 mL in 1 VIAL, SINGLE-DOSE (51662-1659-1)

Marketing

Marketing Status
Marketed Since 2023-07-30
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": "19b0603b-2420-f439-e063-6294a90ae85f", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1725059"], "spl_set_id": ["19b0603b-241f-f439-e063-6294a90ae85f"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 VIAL, SINGLE-DOSE in 1 CARTON (51662-1659-2)  / .1 mL in 1 VIAL, SINGLE-DOSE (51662-1659-1)", "package_ndc": "51662-1659-2", "marketing_start_date": "20230730"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "51662-1659_19b0603b-2420-f439-e063-6294a90ae85f", "dosage_form": "SPRAY", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "51662-1659", "generic_name": "NALOXONE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20230730", "listing_expiration_date": "20261231"}