NDC Package 52565-023-29 Betamethasone Dipropionate

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
52565-023-29
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 30 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Betamethasone Dipropionate
Usage Information:
This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Betamethasone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a strong corticosteroid.
11-Digit NDC Billing Format:
52565002329
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 848178 - betamethasone 0.05 % (betamethasone diproprionate 0.64 MG/ML) Augmented Topical Lotion
  • RxCUI: 848178 - Augmented betamethasone 0.5 MG/ML Topical Lotion
  • RxCUI: 848178 - augmented betamethasone 0.05 % Topical Lotion
  • Labeler Name:
    Teligent Pharma, Inc.
    Sample Package:
    No
    Start Marketing Date:
    02-14-2018
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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
    52565-023-591 BOTTLE, PLASTIC in 1 CARTON / 60 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52565-023-29?

    The NDC Packaged Code 52565-023-29 is assigned to a package of 1 bottle, plastic in 1 carton / 30 ml in 1 bottle, plastic of Betamethasone Dipropionate, labeled by Teligent Pharma, Inc.. The product's dosage form is and is administered via form.

    Is NDC 52565-023 included in the NDC Directory?

    No, Betamethasone Dipropionate with product code 52565-023 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Teligent Pharma, Inc. on February 14, 2018 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 52565-023-29?

    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 52565-023-29?

    The 11-digit format is 52565002329. 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
    5-3-252565-023-295-4-252565-0023-29