NDC 68462-827
Sucralfate oral suspension 1 g per 10 mL suspension
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PPL Healthcare LLC | Sellersville, PA, United States | Makes it and tests it | Problems found, fixed voluntarilyMay 8, 2026 · 9 inspections |
Product details
- Generic drug
- Sucralfate: every company that makes it
- Form
- suspension, oral
- Strength
- 1 g per 10 mL
- Approval
- ANDA ANDA212141
- On the market since
- Jan 5, 2026
- Package NDCs
68462-827-61- Official label
- DailyMed (National Library of Medicine), updated Jan 6, 2026
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