NDC 0121-0965

Lactulose 10 g per 10 g powder, for solution

On the label: Pharmaceutical Associates, 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 Pharmaceutical Associates, Inc. names for other drugs.

Product details

Generic drug
Lactulose: every company that makes it
Form
powder, for solution, oral
Strength
10 g per 10 g
Approval
ANDA ANDA217914
On the market since
Mar 17, 2025
Package NDCs
0121-0965-01 0121-0965-30
Official label
DailyMed (National Library of Medicine), updated Jul 7, 2026

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