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  5. NDC Package Code: 72572-450-25 Naloxone Hydrochloride

NDC Package 72572-450-25 Naloxone Hydrochloride

Nalxone Hydrochloride Injection 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:
72572-450-25
Package Description:
25 VIAL in 1 CARTON / 1 mL in 1 VIAL (72572-450-01)
Product Code:
72572-450
Proprietary Name:
Naloxone Hydrochloride
Non-Proprietary Name:
Nalxone Hydrochloride
Substance Name:
Naloxone Hydrochloride
Usage Information:
Naloxone Hydrochloride Injection, USP 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 Injection, USP is also indicated for diagnosis of suspected or known acute opioid overdosage.Naloxone Hydrochloride Injection, USP may be useful as an adjunctive agent to increase blood pressure in the management of septic shock (see CLINICAL PHARMACOLOGY; Adjunctive Use in Septic Shock).
11-Digit NDC Billing Format:
72572045025
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1191222 - naloxone HCl 0.4 MG/ML Injectable Solution
  • RxCUI: 1191222 - naloxone hydrochloride 0.4 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Civica, Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    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:
    ANDA070299
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-11-2019
    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 72572-450-25 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    72572045025J2310Inj naloxone hydrochloride1 MG1250.410

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 72572-450-25?

    The NDC Packaged Code 72572-450-25 is assigned to a package of 25 vial in 1 carton / 1 ml in 1 vial (72572-450-01) of Naloxone Hydrochloride, a human prescription drug labeled by Civica, Inc.. The product's dosage form is injection and is administered via intramuscular; intravenous; subcutaneous form.

    Is NDC 72572-450 included in the NDC Directory?

    Yes, Naloxone Hydrochloride with product code 72572-450 is active and included in the NDC Directory. The product was first marketed by Civica, Inc. on November 11, 2019 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 NDC billing unit for package 72572-450-25?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 72572-450-25?

    The 11-digit format is 72572045025. 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 5-3-2 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
    5-3-272572-450-255-4-272572-0450-25