NDC Package 51013-426-48 Stool Softener

Docusate Sodium Capsule, Liquid Filled 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:
51013-426-48
Package Description:
1 BOTTLE in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code:
Proprietary Name:
Stool Softener
Non-Proprietary Name:
Docusate Sodium
Substance Name:
Docusate Sodium
Usage Information:
This medication is used to treat occasional constipation. Some medications and conditions can make constipation more likely. Stool softeners such as docusate are often the first method used for preventing and treating this type of constipation. Docusate is often used when straining to have a bowel movement should be avoided (e.g., after a heart attack or surgery). Docusate is a stool softener. It works by increasing the amount of water the stool absorbs in the gut, making the stool softer and easier to pass.
11-Digit NDC Billing Format:
51013042648
NDC to RxNorm Crosswalk:
  • RxCUI: 1115005 - docusate sodium 100 MG Oral Capsule
  • RxCUI: 1115005 - DOSS Sodium 100 MG Oral Capsule
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Puracap Pharmaceutical Llc
    Dosage Form:
    Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
    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:
    02-12-2018
    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 51013-426-48?

    The NDC Packaged Code 51013-426-48 is assigned to a package of 1 bottle in 1 carton / 10 capsule, liquid filled in 1 bottle of Stool Softener, a human over the counter drug labeled by Puracap Pharmaceutical Llc. The product's dosage form is capsule, liquid filled and is administered via oral form.

    Is NDC 51013-426 included in the NDC Directory?

    Yes, Stool Softener with product code 51013-426 is active and included in the NDC Directory. The product was first marketed by Puracap Pharmaceutical Llc on February 12, 2018 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 51013-426-48?

    The 11-digit format is 51013042648. 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
    5-3-251013-426-485-4-251013-0426-48