NDC Package 69539-129-30 Pregabalin

Tablet, Film Coated, Extended Release 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:
69539-129-30
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
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:
69539012930
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:
    Msn Laboratories Private Limited
    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):
    DEA Schedule:
    Schedule V (CV) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA213226
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-13-2021
    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.

    Frequently Asked Questions

    What is NDC 69539-129-30?

    The NDC Packaged Code 69539-129-30 is assigned to a package of 30 tablet, film coated, extended release in 1 bottle of Pregabalin, a human prescription drug labeled by Msn Laboratories Private Limited. The product's dosage form is tablet, film coated, extended release and is administered via oral form.

    Is NDC 69539-129 included in the NDC Directory?

    Yes, Pregabalin with product code 69539-129 is active and included in the NDC Directory. The product was first marketed by Msn Laboratories Private Limited on April 13, 2021 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 69539-129-30?

    The 11-digit format is 69539012930. 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
    5-3-269539-129-305-4-269539-0129-30