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  5. NDC Package Code: 0228-2637-00 Gabapentin

NDC Package 0228-2637-00 Gabapentin

Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

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

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
0228-2637-00
Package Description:
10800 TABLET, FILM COATED in 1 BAG
Product Code:
0228-2637
Proprietary Name:
Gabapentin
Non-Proprietary Name:
Gabapentin
Substance Name:
Gabapentin
Usage Information:
Gabapentin is used with other medications to prevent and control seizures. It is also used to relieve nerve pain following shingles (a painful rash due to herpes zoster infection) in adults. Gabapentin is known as an anticonvulsant or antiepileptic drug.
11-Digit NDC Billing Format:
00228263700
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Actavis Pharma, Inc.
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Decreased Central Nervous System Disorganized Electrical Activity - [PE] (Physiologic Effect)
Sample Package:
N/A
FDA Application Number:
ANDA075694
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-04-2004
End Marketing Date:
07-31-2025
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
0228-2637-11100 TABLET, FILM COATED in 1 BOTTLE
0228-2637-50500 TABLET, FILM COATED in 1 BOTTLE
0228-2637-7712864 TABLET, FILM COATED in 1 CONTAINER

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0228-2637-00?

The NDC Packaged Code 0228-2637-00 is assigned to a package of 10800 tablet, film coated in 1 bag of Gabapentin, a human prescription drug labeled by Actavis Pharma, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 0228-2637 included in the NDC Directory?

Yes, Gabapentin with product code 0228-2637 is active and included in the NDC Directory. The product was first marketed by Actavis Pharma, Inc. on October 04, 2004.

What is the 11-digit format for NDC 0228-2637-00?

The 11-digit format is 00228263700. 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
4-4-20228-2637-005-4-200228-2637-00