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  5. NDC Package Code: 41250-665-04 Meijer Gentle Laxative

NDC Package 41250-665-04 Meijer Gentle Laxative

Bisacodyl Suppository Rectal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
41250-665-04
Package Description:
1 BLISTER PACK in 1 CARTON / 40 mg in 1 BLISTER PACK
Product Code:
41250-665
Proprietary Name:
Meijer Gentle 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:
41250066504
NDC to RxNorm Crosswalk:
  • RxCUI: 198509 - bisacodyl 10 MG Rectal Suppository
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Meijer Distribution Inc.
    Dosage Form:
    Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
    Administration Route(s):
  • Rectal - Administration to the rectum.
    • Active Ingredient(s):
  • BISACODYL 10 mg/2000mg
    • Pharmacologic Class(es):
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Stimulant Laxative - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • 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:
    02-26-2020
    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 41250-665-04?

    The NDC Packaged Code 41250-665-04 is assigned to a package of 1 blister pack in 1 carton / 40 mg in 1 blister pack of Meijer Gentle Laxative, a human over the counter drug labeled by Meijer Distribution Inc.. The product's dosage form is suppository and is administered via rectal form.

    Is NDC 41250-665 included in the NDC Directory?

    Yes, Meijer Gentle Laxative with product code 41250-665 is active and included in the NDC Directory. The product was first marketed by Meijer Distribution Inc. on February 26, 2020 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 41250-665-04?

    The 11-digit format is 41250066504. 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
    5-3-241250-665-045-4-241250-0665-04