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  5. NDC Package Code: 55154-4747-5 Labetalol Hydrochloride

NDC Package 55154-4747-5 Labetalol Hydrochloride

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

Table of Contents

    1. Package Information
    2. 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:
55154-4747-5
Package Description:
5 CARTRIDGE in 1 BAG / 4 mL in 1 CARTRIDGE
Product Code:
55154-4747
Proprietary Name:
Labetalol Hydrochloride
Non-Proprietary Name:
Labetalol Hydrochloride
Substance Name:
Labetalol Hydrochloride
Usage Information:
Labetalol HCl injection is indicated for control of blood pressure in severe hypertension.
11-Digit NDC Billing Format:
55154474705
NDC to RxNorm Crosswalk:
  • RxCUI: 1234256 - labetalol HCl 20 MG in 4 ML Cartridge
  • RxCUI: 1234256 - 4 ML labetalol hydrochloride 5 MG/ML Cartridge
  • RxCUI: 1234256 - labetalol HCl 20 MG per 4 ML Cartridge
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cardinal Health 107, Llc
    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):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • LABETALOL HYDROCHLORIDE 5 mg/mL
    • Pharmacologic Class(es):
  • Adrenergic beta-Antagonists - [MoA] (Mechanism of Action)
  • beta-Adrenergic Blocker - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA075239
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-29-1999
    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.

    Frequently Asked Questions

    What is NDC 55154-4747-5?

    The NDC Packaged Code 55154-4747-5 is assigned to a package of 5 cartridge in 1 bag / 4 ml in 1 cartridge of Labetalol Hydrochloride, a human prescription drug labeled by Cardinal Health 107, Llc. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 55154-4747 included in the NDC Directory?

    Yes, Labetalol Hydrochloride with product code 55154-4747 is active and included in the NDC Directory. The product was first marketed by Cardinal Health 107, Llc on November 29, 1999 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 55154-4747-5?

    The 11-digit format is 55154474705. 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
    5-4-155154-4747-55-4-255154-4747-05