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  5. NDC Package Code: 24208-353-05 Alrex

NDC Package 24208-353-05 Alrex

Loteprednol Etabonate Suspension/ Drops Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    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:
24208-353-05
Package Description:
1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Product Code:
24208-353
Proprietary Name:
Alrex
Non-Proprietary Name:
Loteprednol Etabonate
Substance Name:
Loteprednol Etabonate
Usage Information:
This medication is used to temporarily relieve seasonal allergy symptoms of the eyes such as swelling, redness, and itching. Loteprednol belongs to a class of drugs known as corticosteroids.
11-Digit NDC Billing Format:
24208035305
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 213262 - Alrex 0.2 % Ophthalmic Suspension
  • RxCUI: 213262 - loteprednol etabonate 2 MG/ML Ophthalmic Suspension [Alrex]
  • RxCUI: 213262 - Alrex 2 MG/ML Ophthalmic Suspension
  • RxCUI: 311381 - loteprednol etabonate 0.2 % Ophthalmic Suspension
  • RxCUI: 311381 - loteprednol etabonate 2 MG/ML Ophthalmic Suspension
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bausch & Lomb Incorporated
    Dosage Form:
    Suspension/ Drops - A suspension which is usually administered in a dropwise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
    • Active Ingredient(s):
  • LOTEPREDNOL ETABONATE 2 mg/mL
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA020803
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-09-1998
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    24208-353-011 BOTTLE, DROPPER in 1 CARTON / 1 mL in 1 BOTTLE, DROPPER
    24208-353-101 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 24208-353-05?

    The NDC Packaged Code 24208-353-05 is assigned to a package of 1 bottle, dropper in 1 carton / 5 ml in 1 bottle, dropper of Alrex, a human prescription drug labeled by Bausch & Lomb Incorporated. The product's dosage form is suspension/ drops and is administered via ophthalmic form.

    Is NDC 24208-353 included in the NDC Directory?

    Yes, Alrex with product code 24208-353 is active and included in the NDC Directory. The product was first marketed by Bausch & Lomb Incorporated on March 09, 1998 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 24208-353-05?

    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 24208-353-05?

    The 11-digit format is 24208035305. 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
    5-3-224208-353-055-4-224208-0353-05