NDC 60687-738
Sucralfate 1 g per 10 mL suspension
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from VistaPharm, LLC's NDC 66689-305.
Where the pills inside were 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 VistaPharm, LLC names for other drugs.
Recalls
- Oct 18, 2023 · Class I · VistaPharm LLC
Microbial Contamination of Non-Sterile Products: identified as Bacillus cereus.
Lots: Lot#: 810300, Exp 10/2023 - Aug 30, 2023 · Class II · VistaPharm LLC
Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results
Lots: Lot #: 921100; Exp. 02/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sucralfate: every company that makes it
- Form
- suspension, oral
- Strength
- 1 g per 10 mL
- Approval
- ANDA ANDA211884
- On the market since
- Aug 1, 2023
- Package NDCs
60687-738-0860687-738-2360687-738-4260687-738-4860687-738-56- Official label
- DailyMed (National Library of Medicine), updated Aug 10, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?