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  4. NDC Product Code: 59741-249 Lactulose

NDC 59741-249 Lactulose

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59741-249?
  4. Lactulose Uses
  5. Active Ingredients UNII Codes
  6. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59741-249
Proprietary Name:
Lactulose
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bio-pharm, Inc.
Labeler Code:
59741
Product Label ID:
e9734719-07b9-4ac9-b082-be07f4e9a68f
Start Marketing Date: [9]
06-13-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59741-249-09

Package Description: 237 mL in 1 BOTTLE

NDC Code 59741-249-17

Package Description: 473 mL in 1 BOTTLE

NDC Code 59741-249-33

Package Description: 946 mL in 1 BOTTLE

Product Details

What is NDC 59741-249?

The NDC code 59741-249 is assigned by the FDA to the product Lactulose which is product labeled by Bio-pharm, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 59741-249-09 237 ml in 1 bottle , 59741-249-17 473 ml in 1 bottle , 59741-249-33 946 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Lactulose?

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.

Which are Lactulose UNII Codes?

The UNII codes for the active ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Lactulose?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".