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  5. NDC Package Code: 51662-1238-1 Naloxone Hydrochloride

NDC Package 51662-1238-1 Naloxone Hydrochloride

Injection, Solution Intramuscular; Intravenous; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51662-1238-1
Package Description:
1 mL in 1 CARTRIDGE
Product Code:
51662-1238
Proprietary Name:
Naloxone Hydrochloride
Non-Proprietary Name:
Naloxone Hydrochloride
Substance Name:
Naloxone Hydrochloride
Usage Information:
Naloxone hydrochloride injection is indicated for the complete or partial reversal of opioid depression, including respiratory depression, induced by natural and synthetic opioids including propoxyphene, methadone, and certain mixed agonist-antagonist analgesics: nalbuphine, pentazocine, butorphanol, and cyclazocine.Naloxone hydrochloride is also indicated for the diagnosis of suspected or known acute opioid overdosage. Naloxone hydrochloride injection may be useful as an adjunctive agent to increase blood pressure in the management of septic shock (see INDICATIONS & USAGE: Adjunctive Use in Septic Shock).
11-Digit NDC Billing Format:
51662123801
NDC to RxNorm Crosswalk:
  • RxCUI: 1191234 - naloxone HCl 0.4 MG in 1 ML Cartridge
  • RxCUI: 1191234 - 1 ML naloxone hydrochloride 0.4 MG/ML Cartridge
  • RxCUI: 1191234 - naloxone hydrochloride 0.4 MG per 1 ML Cartridge
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co. Llc, Dba Healthfirst
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • NALOXONE HYDROCHLORIDE .4 mg/mL
    • Pharmacologic Class(es):
  • Opioid Antagonist - [EPC] (Established Pharmacologic Class)
  • Opioid Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA070172
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-03-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 51662-1238-1 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    51662123801J2310Inj naloxone hydrochloride1 MG110.40.4

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51662-1238-1?

    The NDC Packaged Code 51662-1238-1 is assigned to a package of 1 ml in 1 cartridge of Naloxone Hydrochloride, a human prescription drug labeled by Hf Acquisition Co. Llc, Dba Healthfirst. The product's dosage form is injection, solution and is administered via intramuscular; intravenous; subcutaneous form.

    Is NDC 51662-1238 included in the NDC Directory?

    Yes, Naloxone Hydrochloride with product code 51662-1238 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co. Llc, Dba Healthfirst on September 03, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51662-1238-1?

    The 11-digit format is 51662123801. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-151662-1238-15-4-251662-1238-01