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  5. NDC Package Code: 85592-819-30 Lactulose Crystalline

NDC Package 85592-819-30 Lactulose Crystalline

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:
85592-819-30
Package Description:
30 POUCH in 1 CARTON / 10 g in 1 POUCH (85592-819-01)
Product Code:
85592-819
Proprietary Name:
Lactulose Crystalline
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:
85592081930
Product Type:
Human Prescription Drug
Labeler Name:
Cumberland Assured Products 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 10 g/10g
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA074712
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-01-2025
Listing Expiration Date:
12-31-2026
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 85592-819-30?

The NDC Packaged Code 85592-819-30 is assigned to a package of 30 pouch in 1 carton / 10 g in 1 pouch (85592-819-01) of Lactulose Crystalline, a human prescription drug labeled by Cumberland Assured Products Inc.. The product's dosage form is powder, for solution and is administered via oral form.

Is NDC 85592-819 included in the NDC Directory?

Yes, Lactulose Crystalline with product code 85592-819 is active and included in the NDC Directory. The product was first marketed by Cumberland Assured Products Inc. on September 01, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85592-819-30?

The 11-digit format is 85592081930. 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
5-3-285592-819-305-4-285592-0819-30