NDC 81033-241
Lactulose Solution 10 g per 15 mL solution
On the label: Kesin Pharma Corporation. It's repackaged: Kesin Pharma Corporation rebottles it from Bajaj Medical, LLC's NDC 61037-471.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bajaj Medical, LLC | Chicago, IL, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyAug 25, 2025 · 4 inspections |
Repackaging site
- Kesin Pharma Corporation, Oldsmar, FL, United States · repackages it
Product details
- Generic drug
- Lactulose: every company that makes it
- Form
- solution, oral; rectal
- Strength
- 10 g per 15 mL
- Approval
- ANDA ANDA076645
- On the market since
- Apr 16, 2021
- Package NDCs
81033-241-1581033-241-3081033-241-5081033-241-51- Official label
- DailyMed (National Library of Medicine), updated Aug 3, 2026
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