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  5. NDC Package Code: 58151-110-10 Dilantin

NDC Package 58151-110-10 Dilantin

Extended Phenytoin Sodium Capsule, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
58151-110-10
Package Description:
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code:
58151-110
Proprietary Name:
Dilantin
Non-Proprietary Name:
Extended Phenytoin Sodium
Substance Name:
Phenytoin Sodium
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:
58151011010
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1000 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 855671 - phenytoin sodium 100 MG Extended Release Oral Capsule
  • RxCUI: 855671 - DPH sodium 100 MG Extended Release Oral Capsule
  • RxCUI: 855673 - Dilantin 100 MG Extended Release Oral Capsule
  • RxCUI: 855673 - phenytoin sodium 100 MG Extended Release Oral Capsule [Dilantin]
  • RxCUI: 855673 - DPH sodium 100 MG Extended Release Oral Capsule [Dilantin]
Product Type:
Human Prescription Drug
Labeler Name:
Viatris Specialty Llc
Dosage Form:
Capsule, Extended Release - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin, and which releases a drug (or drugs) in such a manner to allow a reduction in dosing frequency as compared to that drug (or drugs) presented as a conventional dosage form.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
PHENYTOIN SODIUM 100 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA084349
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-06-2024
Listing Expiration Date:
12-31-2026
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
58151-110-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
58151-110-88100 BLISTER PACK in 1 CARTON / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (58151-110-32)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 58151-110-10?

The NDC Packaged Code 58151-110-10 is assigned to a package of 1000 capsule, extended release in 1 bottle, plastic of Dilantin, a human prescription drug labeled by Viatris Specialty Llc. The product's dosage form is capsule, extended release and is administered via oral form.

Is NDC 58151-110 included in the NDC Directory?

Yes, Dilantin with product code 58151-110 is active and included in the NDC Directory. The product was first marketed by Viatris Specialty Llc on December 06, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 58151-110-10?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1000.

What is the 11-digit format for NDC 58151-110-10?

The 11-digit format is 58151011010. 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 5-3-2 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
5-3-258151-110-105-4-258151-0110-10