NDC 0121-1746

Lactulose 20 g per 30 mL solution

On the label: Pharmaceutical Associates, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI PharmaGreenville, SC, United StatesMakes it No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action

Product details

Generic drug
Lactulose: every company that makes it
Form
solution, oral
Strength
20 g per 30 mL
Approval
ANDA ANDA074623
On the market since
Dec 3, 2019
Package NDCs
0121-1746-00 0121-1746-06 0121-1746-30 0121-1746-40
Official label
DailyMed (National Library of Medicine), updated Sep 15, 2025

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