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  5. NDC Package Code: 61388-123-26 Zingo

NDC Package 61388-123-26 Zingo

Lidocaine Hydrochloride Monohydrate Powder Intradermal - 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:
61388-123-26
Package Description:
12 POWDER in 1 POUCH
Product Code:
61388-123
Proprietary Name:
Zingo
Non-Proprietary Name:
Lidocaine Hydrochloride Monohydrate
Substance Name:
Lidocaine Hydrochloride
Usage Information:
ZINGO is an amide local anesthetic indicated for use on intact skin to provide local analgesia prior to venipuncture or peripheral intravenous cannulation in children 3–18 years of age. (1)ZINGO is indicated for use on intact skin to provide topical local analgesia prior to venipuncture in adults. (1)Important Limitations: For use on intact skin only (1, 2)For external use only (5)
11-Digit NDC Billing Format:
61388012326
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Powder Pharmaceutical Incorporated
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Administration Route(s):
Intradermal - Administration within the dermis.
Active Ingredient(s):
LIDOCAINE HYDROCHLORIDE .5 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA022114
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
11-01-2024
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
61388-123-4848 CARTON in 1 BOX / 12 POWDER in 1 CARTON (61388-123-12)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 61388-123-26?

The NDC Packaged Code 61388-123-26 is assigned to a package of 12 powder in 1 pouch of Zingo, a human prescription drug labeled by Powder Pharmaceutical Incorporated. The product's dosage form is powder and is administered via intradermal form.

Is NDC 61388-123 included in the NDC Directory?

Yes, Zingo with product code 61388-123 is active and included in the NDC Directory. The product was first marketed by Powder Pharmaceutical Incorporated on November 01, 2024 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 11-digit format for NDC 61388-123-26?

The 11-digit format is 61388012326. 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
5-3-261388-123-265-4-261388-0123-26