NDC 68071-1749

Sucralfate 1 g tablet

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.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

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
68071-1749-1
Official label
DailyMed (National Library of Medicine), updated Jul 15, 2024

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