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
0121-0965-010121-0965-30- Official label
- DailyMed (National Library of Medicine), updated Jul 7, 2026
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