naloxone hydrochloride

Generic: naloxone hydrochloride

Labeler: hf acquisition co. llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naloxone hydrochloride
Generic Name naloxone hydrochloride
Labeler hf acquisition co. llc, dba healthfirst
Dosage Form INJECTION
Routes
PARENTERAL
Active Ingredients

naloxone hydrochloride 1 mg/mL

Manufacturer
HF Acquisition Co. LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1239
Product ID 51662-1239_0fcaff2c-afb8-788b-e063-6394a90ade78
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072076
Listing Expiration 2026-12-31
Marketing Start 2018-09-03

Pharmacologic Class

Classes
opioid antagonist [epc] opioid antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621239
Hyphenated Format 51662-1239

Supplemental Identifiers

RxCUI
1191250
UNII
F850569PQR

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name naloxone hydrochloride (source: ndc)
Generic Name naloxone hydrochloride (source: ndc)
Application Number ANDA072076 (source: ndc)
Routes
PARENTERAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 SYRINGE, PLASTIC in 1 BOX (51662-1239-1) / 2 mL in 1 SYRINGE, PLASTIC
  • 10 POUCH in 1 CASE (51662-1239-3) / 1 mL in 1 POUCH (51662-1239-2)
source: ndc

Packages (2)

51662-1239-1 1 SYRINGE, PLASTIC in 1 BOX (51662-1239-1) / 2 mL in 1 SYRINGE, PLASTIC 51662-1239-3 10 POUCH in 1 CASE (51662-1239-3) / 1 mL in 1 POUCH (51662-1239-2)

Ingredients (1)

naloxone hydrochloride (1 mg/mL)

Linked Drug Pages (1)

NALOXONE HYDROCHLORIDE ndc-match (0.9)

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"}