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  5. NDC Package Code: 70121-1657-1 Triamcinolone Acetonide

NDC Package 70121-1657-1 Triamcinolone Acetonide

Injection, Suspension Intra-articular; Intramuscular - 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:
70121-1657-1
Package Description:
1 VIAL in 1 CARTON / 1 mL in 1 VIAL
Product Code:
70121-1657
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:
70121165701
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:
    Amneal Pharmaceuticals Llc
    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):
  • Intra-articular - Administration within a joint.
  • 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:
    ANDA207550
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-11-2017
    Listing Expiration Date:
    12-31-2025
    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
    70121-1657-525 VIAL in 1 CARTON / 1 mL in 1 VIAL

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70121-1657-1?

    The NDC Packaged Code 70121-1657-1 is assigned to a package of 1 vial in 1 carton / 1 ml in 1 vial of Triamcinolone Acetonide, a human prescription drug labeled by Amneal Pharmaceuticals Llc. The product's dosage form is injection, suspension and is administered via intra-articular; intramuscular form.

    Is NDC 70121-1657 included in the NDC Directory?

    Yes, Triamcinolone Acetonide with product code 70121-1657 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Llc on December 11, 2017 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 70121-1657-1?

    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 70121-1657-1?

    The 11-digit format is 70121165701. 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
    5-4-170121-1657-15-4-270121-1657-01