NDC 68999-106
Sucralfate 1 g per 10 mL suspension
On the label: Chartwell Governmental & Specialty RX, LLC..
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 Chartwell Governmental & Specialty RX, LLC. names for other drugs.
Product details
- Generic drug
- Sucralfate: every company that makes it
- Form
- suspension, oral
- Strength
- 1 g per 10 mL
- Approval
- ANDA ANDA211780
- On the market since
- Apr 14, 2025
- Package NDCs
68999-106-1068999-106-24- Official label
- DailyMed (National Library of Medicine), updated Sep 16, 2026
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