NDC Package 0071-2214-35 Dilantin-125

Phenytoin 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:
0071-2214-35
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 237 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Dilantin-125
Non-Proprietary Name:
Phenytoin
Substance 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:
00071221435
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
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Parke-davis Div Of Pfizer 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:
    NDA008762
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    01-06-1953
    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 0071-2214-35?

    The NDC Packaged Code 0071-2214-35 is assigned to a package of 1 bottle, plastic in 1 carton / 237 ml in 1 bottle, plastic of Dilantin-125, a human prescription drug labeled by Parke-davis Div Of Pfizer Inc. The product's dosage form is suspension and is administered via oral form.

    Is NDC 0071-2214 included in the NDC Directory?

    Yes, Dilantin-125 with product code 0071-2214 is active and included in the NDC Directory. The product was first marketed by Parke-davis Div Of Pfizer Inc on January 06, 1953 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 11-digit format for NDC 0071-2214-35?

    The 11-digit format is 00071221435. 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
    4-4-20071-2214-355-4-200071-2214-35