NDC 53808-1052

Omeprazole 20 mg capsule, 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 55111-158.

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
Omeprazole: every company that makes it
Form
capsule, delayed release
Strength
20 mg
Approval
ANDA ANDA075576
On the market since
Jan 1, 2014
Package NDCs
53808-1052-1
Official label
DailyMed (National Library of Medicine), updated Oct 21, 2014

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