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  5. NDC Package Code: 17856-4070-1 Phenytoin

NDC Package 17856-4070-1 Phenytoin

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:
17856-4070-1
Package Description:
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 4 mL in 1 CUP, UNIT-DOSE (17856-4070-2)
Product Code:
17856-4070
Proprietary Name:
Phenytoin
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:
17856407001
NDC to RxNorm Crosswalk:
  • RxCUI: 1313112 - phenytoin 125 MG in 5 mL Oral Suspension
  • RxCUI: 1313112 - phenytoin 25 MG/ML Oral Suspension
  • RxCUI: 1313112 - DPH 25 MG/ML Oral Suspension
  • RxCUI: 1313112 - phenytoin 100 MG per 4 ML Oral Suspension
  • RxCUI: 1313112 - phenytoin 125 MG per 5 ML Oral Suspension
    • Labeler Name:
    Atlantic Biologicals Corp.
    Sample Package:
    No
    Start Marketing Date:
    04-08-2004
    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 17856-4070-1?

    The NDC Packaged Code 17856-4070-1 is assigned to a package of 72 cup, unit-dose in 1 box, unit-dose / 4 ml in 1 cup, unit-dose (17856-4070-2) of Phenytoin, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

    Is NDC 17856-4070 included in the NDC Directory?

    No, Phenytoin with product code 17856-4070 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on April 08, 2004 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 17856-4070-1?

    The 11-digit format is 17856407001. 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
    5-4-117856-4070-15-4-217856-4070-01