NDC Package 63868-908-25 Gentle Laxative Stimulant Laxative

Bisacodyl Tablet, Coated 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:
63868-908-25
Package Description:
1 BLISTER PACK in 1 CARTON / 25 TABLET, COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Gentle Laxative 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:
63868090825
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:
    Quality Choice (chain Drug Marketing Association)
    Dosage Form:
    Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    M007
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-19-2019
    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 63868-908-25?

    The NDC Packaged Code 63868-908-25 is assigned to a package of 1 blister pack in 1 carton / 25 tablet, coated in 1 blister pack of Gentle Laxative Stimulant Laxative, a human over the counter drug labeled by Quality Choice (chain Drug Marketing Association). The product's dosage form is tablet, coated and is administered via oral form.

    Is NDC 63868-908 included in the NDC Directory?

    Yes, Gentle Laxative Stimulant Laxative with product code 63868-908 is active and included in the NDC Directory. The product was first marketed by Quality Choice (chain Drug Marketing Association) on April 19, 2019 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 63868-908-25?

    The 11-digit format is 63868090825. 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
    5-3-263868-908-255-4-263868-0908-25