NDC Package 0071-2418-19 Zarontin

Ethosuximide Solution 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:
0071-2418-19
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 474 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Zarontin
Non-Proprietary Name:
Ethosuximide
Substance Name:
Ethosuximide
Usage Information:
This medication is used alone or with other medications to prevent and control a certain type of seizure (absence or petit mal seizure). It works by controlling the abnormal electrical activity in the brain that occurs during a seizure.
11-Digit NDC Billing Format:
00071241819
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 251322 - ethosuximide 250 MG in 5 mL Oral Solution
  • RxCUI: 251322 - ethosuximide 50 MG/ML Oral Solution
  • RxCUI: 251322 - ethosuximide 250 MG per 5 ML Oral Solution
  • RxCUI: 755357 - Zarontin 250 MG in 5 mL Oral Solution
  • RxCUI: 755357 - ethosuximide 50 MG/ML Oral Solution [Zarontin]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Parke-davis Div Of Pfizer Inc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA080258
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-10-2020
    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 0071-2418-19?

    The NDC Packaged Code 0071-2418-19 is assigned to a package of 1 bottle, plastic in 1 carton / 474 ml in 1 bottle, plastic of Zarontin, a human prescription drug labeled by Parke-davis Div Of Pfizer Inc. The product's dosage form is solution and is administered via oral form.

    Is NDC 0071-2418 included in the NDC Directory?

    Yes, Zarontin with product code 0071-2418 is active and included in the NDC Directory. The product was first marketed by Parke-davis Div Of Pfizer Inc on March 10, 2020 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 0071-2418-19?

    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 0071-2418-19?

    The 11-digit format is 00071241819. 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 4-4-2 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
    4-4-20071-2418-195-4-200071-2418-19