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  5. NDC Package Code: 24208-040-01 Xipere

NDC Package 24208-040-01 Xipere

Triamcinolone Acetonide Injection, Suspension 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:
24208-040-01
Package Description:
1 TRAY in 1 CARTON / 1 VIAL in 1 TRAY / .9 mL in 1 VIAL (24208-040-02)
Product Code:
24208-040
Proprietary Name:
Xipere
Non-Proprietary Name:
Triamcinolone Acetonide
Substance Name:
Triamcinolone Acetonide
Usage Information:
This medication is used in a variety of conditions such as allergic disorders, arthritis, gout, blood diseases, breathing problems, certain cancers, eye diseases, intestinal disorders, collagen and skin diseases. Talk to your doctor about the risks and benefits of triamcinolone, especially if it is to be injected near your spine (epidural). Rare but serious side effects may occur with epidural use. Triamcinolone is known as a corticosteroid hormone (glucocorticoid). It works by decreasing your body's immune response to these diseases and reduces symptoms such as swelling.
11-Digit NDC Billing Format:
24208004001
NDC to RxNorm Crosswalk:
  • RxCUI: 2585221 - triamcinolone acetonide 40 MG in 0.9 ML Injection
  • RxCUI: 2585221 - 0.9 ML triamcinolone acetonide 40 MG/ML Injection
  • RxCUI: 2585221 - triamcinolone acetonide 40 MG per 0.9 ML Injection
  • RxCUI: 2585226 - XIPERE 40 MG in 0.9 ML Injection
  • RxCUI: 2585226 - 0.9 ML triamcinolone acetonide 40 MG/ML Injection [Xipere]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bausch & Lomb Incorporated
    Dosage Form:
    Injection, Suspension - A liquid preparation, suitable for injection, which consists of solid particles dispersed throughout a liquid phase in which the particles are not soluble. It can also consist of an oil phase dispersed throughout an aqueous phase, or vice-versa.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
    • Active Ingredient(s):
  • TRIAMCINOLONE ACETONIDE 40 mg/mL
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    Yes
    FDA Application Number:
    NDA211950
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-17-2021
    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
    24208-040-401 TRAY in 1 CARTON / 1 VIAL in 1 TRAY / .9 mL in 1 VIAL (24208-040-41)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 24208-040-01?

    The NDC Packaged Code 24208-040-01 is assigned to a package of 1 tray in 1 carton / 1 vial in 1 tray / .9 ml in 1 vial (24208-040-02) of Xipere, a human prescription drug labeled by Bausch & Lomb Incorporated. The product's dosage form is injection, suspension and is administered via ophthalmic form.

    Is NDC 24208-040 included in the NDC Directory?

    Yes, Xipere with product code 24208-040 is active and included in the NDC Directory. The product was first marketed by Bausch & Lomb Incorporated on December 17, 2021 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 24208-040-01?

    The 11-digit format is 24208004001. 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
    5-3-224208-040-015-4-224208-0040-01