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  5. NDC Package Code: 42023-179-05 Buprenorphine Hydrochloride

NDC Package 42023-179-05 Buprenorphine Hydrochloride

Injection Intramuscular; Intravenous - 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:
42023-179-05
Package Description:
5 VIAL in 1 CARTON / 1 mL in 1 VIAL
Product Code:
42023-179
Proprietary Name:
Buprenorphine Hydrochloride
Non-Proprietary Name:
Buprenorphine Hydrochloride
Substance Name:
Buprenorphine Hydrochloride
Usage Information:
Buprenorphine hydrochloride injection is indicated for the management of pain severe enough to require an opioid analgesic and for which alternate treatments are inadequate.
11-Digit NDC Billing Format:
42023017905
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 238129 - buprenorphine HCl 0.3 MG in 1 ML Injection
  • RxCUI: 238129 - 1 ML buprenorphine 0.3 MG/ML Injection
  • RxCUI: 238129 - buprenorphine 0.3 MG/ML (as buprenorphine HCl 0.324 MG/ML) Injection
  • RxCUI: 238129 - buprenorphine HCl 0.3 MG per 1 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Par Pharmaceutical, 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.
    • Active Ingredient(s):
  • BUPRENORPHINE HYDROCHLORIDE .324 mg/mL
    • Pharmacologic Class(es):
  • Partial Opioid Agonist - [EPC] (Established Pharmacologic Class)
  • Partial Opioid Agonists - [MoA] (Mechanism of Action)
    • DEA Schedule:
    Schedule III (CIII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA206586
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-30-2015
    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 42023-179-05 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    42023017905J0592Buprenorphine hydrochloride0.1 MG15315

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 42023-179-05?

    The NDC Packaged Code 42023-179-05 is assigned to a package of 5 vial in 1 carton / 1 ml in 1 vial of Buprenorphine Hydrochloride, a human prescription drug labeled by Par Pharmaceutical, Inc.. The product's dosage form is injection and is administered via intramuscular; intravenous form.

    Is NDC 42023-179 included in the NDC Directory?

    Yes, Buprenorphine Hydrochloride with product code 42023-179 is active and included in the NDC Directory. The product was first marketed by Par Pharmaceutical, Inc. on July 30, 2015 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 42023-179-05?

    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 42023-179-05?

    The 11-digit format is 42023017905. 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
    5-3-242023-179-055-4-242023-0179-05