NDC 72189-429

Sucralfate 1 g tablet

On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Nostrum Laboratories, Inc.'s NDC 29033-003.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Nostrum Laboratories, Inc.Bryan, Ohio, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMar 13, 2025 · 6 inspections

Repackaging site

Product details

Generic drug
Sucralfate: every company that makes it
Form
tablet, oral
Strength
1 g
Approval
ANDA ANDA074415
On the market since
Mar 2, 2023
Package NDCs
72189-429-20 72189-429-90
Official label
DailyMed (National Library of Medicine), updated Jan 22, 2025

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