NDC 60432-038 Generlac
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 60432 - Morton Grove Pharmaceuticals, Inc.
- 60432-038 - Generlac
Product Packages
NDC Code 60432-038-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Price per Unit: $0.01286 per ML
NDC Code 60432-038-64
Package Description: 1892 mL in 1 BOTTLE, PLASTIC
Price per Unit: $0.01317 per ML
Product Details
What is NDC 60432-038?
What are the uses for Generlac?
Which are Generlac UNII Codes?
The UNII codes for the active ingredients in this product are:
- LACTULOSE (UNII: 9U7D5QH5AE)
- LACTULOSE (UNII: 9U7D5QH5AE) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Generlac?
- 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
- RxCUI: 544455 - GENERLAC 10 GM in 15 mL Oral Solution
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Patient Education
Lactulose
Lactulose is a synthetic sugar used to treat constipation. It is broken down in the colon into products that pull water out from the body and into the colon. This water softens stools. Lactulose is also used to reduce the amount of ammonia in the blood of patients with liver disease. It works by drawing ammonia from the blood into the colon where it is removed from the body. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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[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".