1. Home
  2. Labeler Index
  3. Remedyrepack Inc.
  4. 70518-0980
  5. NDC Package Code: 70518-0980-1 Dilantin

NDC Package 70518-0980-1 Dilantin

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
70518-0980-1
Package Description:
100 POUCH in 1 BOX / 1 CAPSULE, EXTENDED RELEASE in 1 POUCH (70518-0980-2)
Product Code:
70518-0980
Proprietary Name:
Dilantin
Usage Information:
Phenytoin is used to prevent and control seizures (also called an anticonvulsant or antiepileptic drug). It works by reducing the spread of seizure activity in the brain.
11-Digit NDC Billing Format:
70518098001
NDC to RxNorm Crosswalk:
  • RxCUI: 855869 - phenytoin sodium 30 MG Extended Release Oral Capsule
  • RxCUI: 855869 - DPH sodium 30 MG Extended Release Oral Capsule
  • RxCUI: 855871 - Dilantin 30 MG Extended Release Oral Capsule
  • RxCUI: 855871 - phenytoin sodium 30 MG Extended Release Oral Capsule [Dilantin]
  • RxCUI: 855871 - DPH sodium 30 MG Extended Release Oral Capsule [Dilantin]
    • Labeler Name:
    Remedyrepack Inc.
    Sample Package:
    No
    Start Marketing Date:
    01-22-2018
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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 70518-0980-1?

    The NDC Packaged Code 70518-0980-1 is assigned to a package of 100 pouch in 1 box / 1 capsule, extended release in 1 pouch (70518-0980-2) of Dilantin, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

    Is NDC 70518-0980 included in the NDC Directory?

    No, Dilantin with product code 70518-0980 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Remedyrepack Inc. on January 22, 2018 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70518-0980-1?

    The 11-digit format is 70518098001. 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
    5-4-170518-0980-15-4-270518-0980-01