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  5. NDC Package Code: 81298-5781-5 Triamcinolone Acetonide

NDC Package 81298-5781-5 Triamcinolone Acetonide

Suspension Intra-arterial; Intramuscular - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    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:
81298-5781-5
Package Description:
25 VIAL, SINGLE-USE in 1 CARTON / 1 mL in 1 VIAL, SINGLE-USE (81298-5781-1)
Product Code:
81298-5781
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:
81298578105
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1085754 - triamcinolone acetonide 40 MG/ML Injectable Suspension
  • RxCUI: 1792144 - triamcinolone acetonide 40 MG in 1 ML Injection
  • RxCUI: 1792144 - 1 ML triamcinolone acetonide 40 MG/ML Injection
  • RxCUI: 1792144 - triamcinolone acetonide 40 MG per 1 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Long Grove Pharmaceuticals, Llc
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Intra-arterial - Administration within an artery or arteries.
  • Intramuscular - Administration within a muscle.
    • 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:
    No
    FDA Application Number:
    ANDA213543
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-02-2022
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 81298-5781-5 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    81298578105J3301Triamcinolone acet inj nos10 MG1254100

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 81298-5781-5?

    The NDC Packaged Code 81298-5781-5 is assigned to a package of 25 vial, single-use in 1 carton / 1 ml in 1 vial, single-use (81298-5781-1) of Triamcinolone Acetonide, a human prescription drug labeled by Long Grove Pharmaceuticals, Llc. The product's dosage form is suspension and is administered via intra-arterial; intramuscular form.

    Is NDC 81298-5781 included in the NDC Directory?

    Yes, Triamcinolone Acetonide with product code 81298-5781 is active and included in the NDC Directory. The product was first marketed by Long Grove Pharmaceuticals, Llc on May 02, 2022 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 81298-5781-5?

    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 81298-5781-5?

    The 11-digit format is 81298578105. 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
    5-4-181298-5781-55-4-281298-5781-05