NDC Package 52652-8001-1 Zonisade

Zonisamide Suspension Oral - 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:
52652-8001-1
Package Description:
1 BOTTLE in 1 CARTON / 150 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Zonisade
Non-Proprietary Name:
Zonisamide
Substance Name:
Zonisamide
Usage Information:
Zonisamide is used with other medications to prevent and control seizures (epilepsy). Zonisamide is a sulfonamide anticonvulsant and a carbonic anhydrase inhibitor. It is unknown how zonisamide works to prevent seizures.
11-Digit NDC Billing Format:
52652800101
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2606782 - zonisamide 100 MG in 5 mL Oral Suspension
  • RxCUI: 2606782 - zonisamide 20 MG/ML Oral Suspension
  • RxCUI: 2606782 - zonisamide 100 MG per 5 ML Oral Suspension
  • RxCUI: 2606788 - ZONISADE 100 MG in 5 mL Oral Suspension
  • RxCUI: 2606788 - zonisamide 20 MG/ML Oral Suspension [Zonisade]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Azurity Phramaceuticals, Inc.
    Dosage Form:
    Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA214273
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    07-15-2022
    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.

    Frequently Asked Questions

    What is NDC 52652-8001-1?

    The NDC Packaged Code 52652-8001-1 is assigned to a package of 1 bottle in 1 carton / 150 ml in 1 bottle of Zonisade, a human prescription drug labeled by Azurity Phramaceuticals, Inc.. The product's dosage form is suspension and is administered via oral form.

    Is NDC 52652-8001 included in the NDC Directory?

    Yes, Zonisade with product code 52652-8001 is active and included in the NDC Directory. The product was first marketed by Azurity Phramaceuticals, Inc. on July 15, 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 52652-8001-1?

    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 52652-8001-1?

    The 11-digit format is 52652800101. 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
    5-4-152652-8001-15-4-252652-8001-01