NDC 53808-1007

Pantoprazole 40 mg tablet, delayed release

On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-333.

India: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Pantoprazole: every company that makes it
Form
tablet, delayed release
Strength
40 mg
Approval
ANDA ANDA077619
On the market since
Nov 1, 2014
Package NDCs
53808-1007-1
Official label
DailyMed (National Library of Medicine), updated Jan 17, 2015

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