NDC 69339-209
Sucralfate 1 g per 10 mL suspension
On the label: Natco Pharma USA LLC. It's repackaged: Natco Pharma USA LLC rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-0974.
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 Pharmaceutical Associates, Inc. names for other drugs.
Repackaging site
- Natco Pharma USA LLC, Parsippany, NJ, United States · repackages it
Product details
- Generic drug
- Sucralfate: every company that makes it
- Form
- suspension
- Strength
- 1 g per 10 mL
- Approval
- ANDA ANDA211884
- On the market since
- Aug 1, 2024
- Package NDCs
69339-209-0169339-209-1769339-209-19- Official label
- DailyMed (National Library of Medicine), updated Jul 3, 2024
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