NDC Package 49483-003-52 Stimulant Laxative

Bisacodyl Tablet, Delayed 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:
49483-003-52
Package Description:
25 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Stimulant Laxative
Non-Proprietary Name:
Bisacodyl
Substance Name:
Bisacodyl
Usage Information:
Bisacodyl is used to treat constipation. It may also be used to clean out the intestines before a bowel examination/surgery. Bisacodyl is known as a stimulant laxative. It works by increasing the movement of the intestines, helping the stool to come out.
11-Digit NDC Billing Format:
49483000352
NDC to RxNorm Crosswalk:
  • RxCUI: 308753 - bisacodyl 5 MG Delayed Release Oral Tablet
  • RxCUI: 308753 - bisacodyl 5 MG Enteric Coated Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Time Cap Laboratories, Inc.
    Dosage Form:
    Tablet, Delayed Release - A solid dosage form which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    part334
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    04-01-2014
    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
    49483-003-00100000 TABLET, DELAYED RELEASE in 1 CARTON
    49483-003-01100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
    49483-003-101000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49483-003-52?

    The NDC Packaged Code 49483-003-52 is assigned to a package of 25 tablet, delayed release in 1 blister pack of Stimulant Laxative, a human over the counter drug labeled by Time Cap Laboratories, Inc.. The product's dosage form is tablet, delayed release and is administered via oral form.

    Is NDC 49483-003 included in the NDC Directory?

    Yes, Stimulant Laxative with product code 49483-003 is active and included in the NDC Directory. The product was first marketed by Time Cap Laboratories, Inc. on April 01, 2014 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 49483-003-52?

    The 11-digit format is 49483000352. 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
    5-3-249483-003-525-4-249483-0003-52