NDC Package 51672-1365-2 Fluocinolone Acetonide

Solution Topical - View Billable Units, 11-Digit Format, RxNorm

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:
51672-1365-2
Package Description:
1 BOTTLE in 1 CARTON / 20 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Fluocinolone Acetonide
Non-Proprietary Name:
Fluocinolone Acetonide
Substance Name:
Fluocinolone Acetonide
Usage Information:
This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Fluocinolone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a medium-strength corticosteroid.
11-Digit NDC Billing Format:
51672136502
NDC to RxNorm Crosswalk:
  • RxCUI: 1191310 - fluocinolone acetonide 0.01 % Topical Solution
  • RxCUI: 1191310 - fluocinolone acetonide 0.1 MG/ML Topical Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Taro Pharmaceuticals U.s.a., Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA089124
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-27-2015
    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
    51672-1365-41 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51672-1365-2?

    The NDC Packaged Code 51672-1365-2 is assigned to a package of 1 bottle in 1 carton / 20 ml in 1 bottle of Fluocinolone Acetonide, a human prescription drug labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is solution and is administered via topical form.

    Is NDC 51672-1365 included in the NDC Directory?

    Yes, Fluocinolone Acetonide with product code 51672-1365 is active and included in the NDC Directory. The product was first marketed by Taro Pharmaceuticals U.s.a., Inc. on March 27, 2015 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 51672-1365-2?

    The 11-digit format is 51672136502. 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
    5-4-151672-1365-25-4-251672-1365-02