NDC 73352-905

Lactulose 20 g per 20 g powder, for solution

On the label: Trifluent Pharma, Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Trifluent Pharma, Inc. names for other drugs.

Product details

Generic drug
Lactulose: every company that makes it
Form
powder, for solution, oral
Strength
20 g per 20 g
Approval
ANDA ANDA217914
On the market since
Sep 13, 2025
Package NDCs
73352-905-01 73352-905-15
Official label
DailyMed (National Library of Medicine), updated Sep 13, 2025

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