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  5. NDC Package Code: 66220-729-30 Kristalose

NDC Package 66220-729-30 Kristalose

Lactulose Powder, For Solution Oral - 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:
66220-729-30
Package Description:
30 POUCH in 1 CARTON / 20 g in 1 POUCH (66220-729-01)
Product Code:
66220-729
Proprietary Name:
Kristalose
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:
66220072930
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1251190 - lactulose 10 GM Powder for Oral Solution
  • RxCUI: 1251190 - lactulose 10000 MG Powder for Oral Solution
  • RxCUI: 1251190 - lactulose 10 GM Granules for Oral Solution
  • RxCUI: 1251192 - Kristalose 10 GM Powder for Oral Solution
  • RxCUI: 1251192 - lactulose 10000 MG Powder for Oral Solution [Kristalose]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cumberland Pharmaceuticals Inc.
    Dosage Form:
    Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • LACTULOSE 20 g/20g
    • Pharmacologic Class(es):
  • Acidifying Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    ANDA074712
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-20-2012
    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 66220-729-30?

    The NDC Packaged Code 66220-729-30 is assigned to a package of 30 pouch in 1 carton / 20 g in 1 pouch (66220-729-01) of Kristalose, a human prescription drug labeled by Cumberland Pharmaceuticals Inc.. The product's dosage form is powder, for solution and is administered via oral form.

    Is NDC 66220-729 included in the NDC Directory?

    Yes, Kristalose with product code 66220-729 is active and included in the NDC Directory. The product was first marketed by Cumberland Pharmaceuticals Inc. on January 20, 2012 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 NDC billing unit for package 66220-729-30?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 66220-729-30?

    The 11-digit format is 66220072930. 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
    5-3-266220-729-305-4-266220-0729-30