1. Home
  2. Labeler Index
  3. Golden State Medical Supply, Inc.
  4. 51407-982
  5. NDC Package Code: 51407-982-10 Phenytoin Sodium

NDC Package 51407-982-10 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:
51407-982-10
Package Description:
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Code:
51407-982
Proprietary Name:
Phenytoin Sodium
Non-Proprietary Name:
Phenytoin Sodium
Substance Name:
Phenytoin Sodium
Usage Information:
Extended phenytoin sodium capsules are indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery.
11-Digit NDC Billing Format:
51407098210
NDC to RxNorm Crosswalk:
  • RxCUI: 855671 - phenytoin sodium 100 MG Extended Release Oral Capsule
  • RxCUI: 855671 - DPH sodium 100 MG Extended Release Oral Capsule
Product Type:
Human Prescription Drug
Labeler Name:
Golden State Medical Supply, Inc.
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:
ANDA040684
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-05-2006
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
51407-982-01100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 51407-982-10?

The NDC Packaged Code 51407-982-10 is assigned to a package of 1000 capsule, extended release in 1 bottle of Phenytoin Sodium, a human prescription drug labeled by Golden State Medical Supply, Inc.. The product's dosage form is capsule, extended release and is administered via oral form.

Is NDC 51407-982 included in the NDC Directory?

Yes, Phenytoin Sodium with product code 51407-982 is active and included in the NDC Directory. The product was first marketed by Golden State Medical Supply, Inc. on September 05, 2006 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 11-digit format for NDC 51407-982-10?

The 11-digit format is 51407098210. 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
5-3-251407-982-105-4-251407-0982-10