NDC 87063-176
Sucralfate 1 g tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-2210.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Sucralfate: every company that makes it
- Form
- tablet, oral
- Strength
- 1 g
- Approval
- ANDA ANDA070848
- On the market since
- Nov 11, 1996
- Package NDCs
87063-176-0187063-176-0587063-176-1287063-176-3087063-176-6087063-176-90- Official label
- DailyMed (National Library of Medicine), updated May 18, 2026
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