NDC 55111-332

Pantoprazole 20 mg tablet, delayed release

On the label: Dr.Reddy's Laboratories Ltd..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Dr. Reddy's Laboratories LimitedMedchal-Malkajgiri, IndiaMakes it and tests it Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections

Product details

Generic drug
Pantoprazole: every company that makes it
Form
tablet, delayed release, oral
Strength
20 mg
Approval
ANDA ANDA077619
On the market since
Jan 19, 2011
Package NDCs
55111-332-01 55111-332-05 55111-332-10 55111-332-30 55111-332-78 55111-332-79 55111-332-81 55111-332-90
Official label
DailyMed (National Library of Medicine), updated Aug 30, 2023

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