NDC Package 81033-241-50 Lactulose Solution

Lactulose Solution Usp,10 G/15 Ml Solution Oral; Rectal - 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:
81033-241-50
Package Description:
100 CUP, UNIT-DOSE in 1 CASE / 15 mL in 1 CUP, UNIT-DOSE (81033-241-15)
Product Code:
Proprietary Name:
Lactulose Solution
Non-Proprietary Name:
Lactulose Solution Usp, 10 G/15 Ml
Substance Name:
Lactulose
Usage Information:
This medication is a laxative used to treat constipation. It may help to increase the number of bowel movements per day and the number of days you have a bowel movement. Lactulose is a colonic acidifier that works by increasing stool water content and softening the stool. It is a man-made sugar solution.
11-Digit NDC Billing Format:
81033024150
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Kesin Pharma Corporation
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Rectal - Administration to the rectum.
  • Oral - Administration to or by way of the mouth.
  • Rectal - Administration to the rectum.
Sample Package:
No
FDA Application Number:
ANDA076645
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-16-2021
Listing Expiration Date:
12-31-2025
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
81033-241-3215 mL in 1 BOTTLE, PLASTIC
81033-241-51100 CUP, UNIT-DOSE in 1 CASE / 30 mL in 1 CUP, UNIT-DOSE (81033-241-30)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 81033-241-50?

The NDC Packaged Code 81033-241-50 is assigned to a package of 100 cup, unit-dose in 1 case / 15 ml in 1 cup, unit-dose (81033-241-15) of Lactulose Solution, a human prescription drug labeled by Kesin Pharma Corporation. The product's dosage form is solution and is administered via oral; rectal form.

Is NDC 81033-241 included in the NDC Directory?

Yes, Lactulose Solution with product code 81033-241 is active and included in the NDC Directory. The product was first marketed by Kesin Pharma Corporation on April 16, 2021 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 81033-241-50?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 81033-241-50?

The 11-digit format is 81033024150. 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
5-3-281033-241-505-4-281033-0241-50