Package 51662-1239-1

Brand: naloxone hydrochloride

Generic: naloxone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1239-1
Digits Only 5166212391
Product NDC 51662-1239
Product ID 51662-1239_0fcaff2c-afb8-788b-e063-6394a90ade78
Description

1 SYRINGE, PLASTIC in 1 BOX (51662-1239-1) / 2 mL in 1 SYRINGE, PLASTIC

Marketing

Marketing Status
Marketed Since 2018-09-03
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": ["PARENTERAL"], "spl_id": "0fcaff2c-afb8-788b-e063-6394a90ade78", "openfda": {"unii": ["F850569PQR"], "rxcui": ["1191250"], "spl_set_id": ["74fc593e-ed47-efae-e053-2991aa0a5997"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE, PLASTIC in 1 BOX (51662-1239-1)  / 2 mL in 1 SYRINGE, PLASTIC", "package_ndc": "51662-1239-1", "marketing_start_date": "20180903"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1239-3)  / 1 mL in 1 POUCH (51662-1239-2)", "package_ndc": "51662-1239-3", "marketing_start_date": "20201027"}], "brand_name": "NALOXONE HYDROCHLORIDE", "product_id": "51662-1239_0fcaff2c-afb8-788b-e063-6394a90ade78", "dosage_form": "INJECTION", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "51662-1239", "generic_name": "NALOXONE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co. LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA072076", "marketing_category": "ANDA", "marketing_start_date": "20180903", "listing_expiration_date": "20261231"}