1. Home
  2. Labeler Index
  3. Hikma Pharmaceuticals Usa Inc.
  4. 0143-9551
  5. NDC Package Code: 0143-9551-10 Daunorubicin Hydrochloride

NDC Package 0143-9551-10 Daunorubicin Hydrochloride

Injection 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:
0143-9551-10
Package Description:
10 VIAL in 1 BOX / 4 mL in 1 VIAL (0143-9551-01)
Product Code:
0143-9551
Proprietary Name:
Daunorubicin Hydrochloride
Non-Proprietary Name:
Daunorubicin Hydrochloride
Substance Name:
Daunorubicin Hydrochloride
Usage Information:
Daunorubicin hydrochloride in combination with other approved anticancer drugs is indicated for remission induction in acute nonlymphocytic leukemia (myelogenous, monocytic, erythroid) of adults and for remission induction in acute lymphocytic leukemia of children and adults.
11-Digit NDC Billing Format:
00143955110
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2002002 - DAUNOrubicin 50 MG in 10 ML Injection
  • RxCUI: 2002002 - 10 ML daunorubicin 5 MG/ML Injection
  • RxCUI: 2002002 - daunorubicin (as daunorubicin hydrochloride 5.34 MG) 50 MG per 10 ML Injection
  • RxCUI: 309650 - DAUNOrubicin HCl 20 MG in 4 ML Injection
  • RxCUI: 309650 - 4 ML daunorubicin 5 MG/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hikma Pharmaceuticals Usa 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):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • DAUNORUBICIN HYDROCHLORIDE 5 mg/mL
    • Pharmacologic Class(es):
  • Anthracycline Topoisomerase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Anthracyclines - [CS]
  • Topoisomerase Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA050731
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    01-02-2018
    Listing Expiration Date:
    12-31-2025
    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 0143-9551-10 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00143955110J9150Daunorubicin injection10 MG410220

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0143-9551-10?

    The NDC Packaged Code 0143-9551-10 is assigned to a package of 10 vial in 1 box / 4 ml in 1 vial (0143-9551-01) of Daunorubicin Hydrochloride, a human prescription drug labeled by Hikma Pharmaceuticals Usa Inc.. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 0143-9551 included in the NDC Directory?

    Yes, Daunorubicin Hydrochloride with product code 0143-9551 is active and included in the NDC Directory. The product was first marketed by Hikma Pharmaceuticals Usa Inc. on January 02, 2018 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0143-9551-10?

    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 0143-9551-10?

    The 11-digit format is 00143955110. 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 4-4-2 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
    4-4-20143-9551-105-4-200143-9551-10