NDC 81033-149
Sucralfate 1 g per 10 mL suspension
On the label: Kesin Pharma Corporation. It's repackaged: Kesin Pharma Corporation rebottles it from Strides Pharma Science Limited's NDC 64380-149.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Strides Pharma Science Limited | Bengaluru, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 20, 2026 · 11 inspections |
Repackaging site
- Kesin Pharma Corporation, Oldsmar, FL, United States · packages it, labels it and repackages it
Product details
- Generic drug
- Sucralfate: every company that makes it
- Form
- suspension, oral
- Strength
- 1 g per 10 mL
- Approval
- ANDA ANDA216474
- On the market since
- Jul 1, 2024
- Package NDCs
81033-149-1081033-149-4481033-149-52- Official label
- DailyMed (National Library of Medicine), updated Jul 1, 2025
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