NDC 72189-234

Sucralfate 1 g tablet

On the label: Direct Rx. It's repackaged: Direct Rx 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
Jun 18, 2021
Package NDCs
72189-234-20 72189-234-90
Official label
DailyMed (National Library of Medicine), updated Jan 20, 2025

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?