NDC Package 50268-497-01 Pregabalin

Capsule 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:
50268-497-01
Package Description:
100 BLISTER PACK in 1 BOX / 1 CAPSULE in 1 BLISTER PACK (50268-497-11)
Product Code:
Proprietary Name:
Pregabalin
Non-Proprietary Name:
Pregabalin
Substance Name:
Pregabalin
Usage Information:
This medication is used to treat pain caused by nerve damage due to diabetes, shingles (herpes zoster) infection, or spinal cord injury. This medication is also used to treat pain in people with fibromyalgia. It is also used with other medications to treat certain types of seizures (focal seizures).
11-Digit NDC Billing Format:
50268049701
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Avpak
Dosage Form:
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
DEA Schedule:
Schedule V (CV) Substances
Sample Package:
No
FDA Application Number:
ANDA209357
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-09-2025
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.

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Frequently Asked Questions

What is NDC 50268-497-01?

The NDC Packaged Code 50268-497-01 is assigned to a package of 100 blister pack in 1 box / 1 capsule in 1 blister pack (50268-497-11) of Pregabalin, a human prescription drug labeled by Avpak. The product's dosage form is capsule and is administered via oral form.

Is NDC 50268-497 included in the NDC Directory?

Yes, Pregabalin with product code 50268-497 is active and included in the NDC Directory. The product was first marketed by Avpak on October 09, 2025 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 50268-497-01?

The 11-digit format is 50268049701. 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
5-3-250268-497-015-4-250268-0497-01