NDC Package 70720-100-10 Quzyttir

Cetirizine Hydrochloride Injection Intravenous - 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:
Package Description:
1 VIAL, GLASS in 1 CARTON / 1 mL in 1 VIAL, GLASS (70720-100-01)
Product Code:
Proprietary Name:
Non-Proprietary Name:
Cetirizine Hydrochloride
Substance Name:
Cetirizine Hydrochloride
Usage Information:
QUZYTTIR™ is indicated for the treatment of acute urticaria in adults and children 6 months of age and older.
11-Digit NDC Billing Format:
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2261746 - cetirizine hydrochloride 10 MG in 1 ML Injection
  • RxCUI: 2261746 - 1 ML cetirizine hydrochloride 10 MG/ML Injection
  • RxCUI: 2261746 - cetirizine hydrochloride 10 MG per 1 ML Injection
  • RxCUI: 2261754 - QUZYTTIR 10 MG in 1 ML Injection
  • RxCUI: 2261754 - 1 ML cetirizine hydrochloride 10 MG/ML Injection [Quzyttir]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Tersera Therapeutics Llc
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    FDA Application Number:
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    Listing Expiration Date:
    Exclude Flag:
    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
    70720-100-2525 VIAL, GLASS in 1 CARTON / 1 mL in 1 VIAL, GLASS (70720-100-01)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70720-100-10?

    The NDC Packaged Code 70720-100-10 is assigned to a package of 1 vial, glass in 1 carton / 1 ml in 1 vial, glass (70720-100-01) of Quzyttir, a human prescription drug labeled by Tersera Therapeutics Llc. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 70720-100 included in the NDC Directory?

    Yes, Quzyttir with product code 70720-100 is active and included in the NDC Directory. The product was first marketed by Tersera Therapeutics Llc on November 13, 2019 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 70720-100-10?

    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 70720-100-10?

    The 11-digit format is 70720010010. 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