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  5. NDC Package Code: 50228-463-30 Pregabalin Extended Release

NDC Package 50228-463-30 Pregabalin Extended Release

Pregabalin Tablet, Film Coated, 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:
50228-463-30
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
50228-463
Proprietary Name:
Pregabalin Extended Release
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:
50228046330
NDC to RxNorm Crosswalk:
  • RxCUI: 1988974 - pregabalin 165 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1988974 - 24 HR pregabalin 165 MG Extended Release Oral Tablet
  • RxCUI: 1988977 - pregabalin 330 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1988977 - 24 HR pregabalin 330 MG Extended Release Oral Tablet
  • RxCUI: 1988980 - pregabalin 82.5 MG 24HR Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sciegen Pharmaceuticals, Inc.
    Dosage Form:
    Tablet, Film Coated, Extended Release - 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; the tablet is formulated in such manner as to make the contained medicament available over an extended period of time following ingestion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PREGABALIN 165 mg/1
    • DEA Schedule:
    Schedule V (CV) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA215675
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-14-2022
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50228-463-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50228-463-30?

    The NDC Packaged Code 50228-463-30 is assigned to a package of 30 tablet, film coated, extended release in 1 bottle of Pregabalin Extended Release, a human prescription drug labeled by Sciegen Pharmaceuticals, Inc.. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 50228-463 included in the NDC Directory?

    Yes, Pregabalin Extended Release with product code 50228-463 is active and included in the NDC Directory. The product was first marketed by Sciegen Pharmaceuticals, Inc. on September 14, 2022 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 50228-463-30?

    The 11-digit format is 50228046330. 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
    5-3-250228-463-305-4-250228-0463-30