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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 072029

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NDA 072029 describes LACTULOSE, which is a drug marketed by Cumberland Pharms, Ani Pharms, Apozeal Pharms, Aurobindo Pharma Ltd, Chartwell Rx, Fresenius Kabi, Hikma, Lannett Co Inc, Morton Grove, Paco, Pharm Assoc, Vistapharm, Xttrium Labs Inc, Bajaj, Pai Holdings Pharm, Roxane, and Solvay, and is included in twenty-two NDAs. It is available from seventeen suppliers. Additional details are available on the LACTULOSE profile page.

The generic ingredient in LACTULOSE is lactulose. There are twenty drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the lactulose profile page.

Summary for 072029

Tradename:	LACTULOSE
Applicant:	Paco
Ingredient:	lactulose
Patents:	0

Medical Subject Heading (MeSH) Categories for 072029

Gastrointestinal Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	SOLUTION;ORAL, RECTAL			Strength	10GM/15ML
Approval Date:	Aug 25, 1992	TE:		RLD:	No

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