NDC Package 0121-1746-40 Lactulose

Solution 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:
0121-1746-40
Package Description:
4 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (0121-1746-30)
Product Code:
Proprietary Name:
Lactulose
Non-Proprietary Name:
Lactulose
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:
00121174640
NDC to RxNorm Crosswalk:
  • RxCUI: 391937 - lactulose 10 GM in 15 mL Oral Solution
  • RxCUI: 391937 - lactulose 667 MG/ML Oral Solution
  • RxCUI: 391937 - lactulose 10 GM per 15 ML Oral Solution
  • RxCUI: 391937 - lactulose 20 GM per 30 ML Oral Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Pharmaceutical Associates, Inc.
    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.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA074623
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-03-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0121-1746-0010 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE
    0121-1746-066 CARTON in 1 CASE / 16 CUP, UNIT-DOSE in 1 CARTON / 30 mL in 1 CUP, UNIT-DOSE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0121-1746-40?

    The NDC Packaged Code 0121-1746-40 is assigned to a package of 4 tray in 1 case / 10 cup, unit-dose in 1 tray / 30 ml in 1 cup, unit-dose (0121-1746-30) of Lactulose, a human prescription drug labeled by Pharmaceutical Associates, Inc.. The product's dosage form is solution and is administered via oral form.

    Is NDC 0121-1746 included in the NDC Directory?

    Yes, Lactulose with product code 0121-1746 is active and included in the NDC Directory. The product was first marketed by Pharmaceutical Associates, Inc. on December 03, 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 0121-1746-40?

    The 11-digit format is 00121174640. 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 4-4-2 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
    4-4-20121-1746-405-4-200121-1746-40