NDC Package 68788-7814-5 Triamcinolone Acetonide

Paste Dental - 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:
68788-7814-5
Package Description:
1 TUBE in 1 CARTON / 5 g in 1 TUBE
Product Code:
Proprietary Name:
Triamcinolone Acetonide
Non-Proprietary Name:
Triamcinolone Acetonide
Substance Name:
Triamcinolone Acetonide
Usage Information:
This medication is used to treat a variety of skin conditions (e.g., eczema, dermatitis, allergies, rash). Triamcinolone reduces the swelling, itching, and redness that can occur in these types of conditions. This medication is a medium- to strong-potency corticosteroid. The potency depends on the strength and the form that you use. For details on the potency of your product, ask your pharmacist.
11-Digit NDC Billing Format:
68788781405
NDC to RxNorm Crosswalk:
  • RxCUI: 1085728 - triamcinolone acetonide 0.1 % Oral Paste
  • RxCUI: 1085728 - triamcinolone acetonide 0.001 MG/MG Oral Paste
  • RxCUI: 1085728 - triamcinolone acetonide 0.1 % Dental Paste
  • RxCUI: 1085728 - triamcinolone acetonide 1 MG per GM Oral Paste
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Preferred Pharmaceuticals Inc
    Dosage Form:
    Paste - A semisolid3 dosage form, containing a large proportion (20 – 50%) of solids finely dispersed in a fatty vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA070730
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-03-2020
    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 68788-7814-5?

    The NDC Packaged Code 68788-7814-5 is assigned to a package of 1 tube in 1 carton / 5 g in 1 tube of Triamcinolone Acetonide, a human prescription drug labeled by Preferred Pharmaceuticals Inc. The product's dosage form is paste and is administered via dental form.

    Is NDC 68788-7814 included in the NDC Directory?

    Yes, Triamcinolone Acetonide with product code 68788-7814 is active and included in the NDC Directory. The product was first marketed by Preferred Pharmaceuticals Inc on November 03, 2020 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 68788-7814-5?

    The 11-digit format is 68788781405. 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
    5-4-168788-7814-55-4-268788-7814-05