NDC 49999-265

Omeprazole 20 mg capsule, delayed release

On the label: Lake Erie Medical DBA Quality Care Products LLC. It's a repackaged product: Lake Erie Medical DBA Quality Care Products LLC rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-158.

Where the pills inside were made

Dr. Reddy's Laboratories Limited

Medchal-Malkajgiri, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Oct 27, 2023. 8 inspections on record.

Repackaging site

• Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC, · repackages it

Product details

Generic drug

Omeprazole: see every company that makes it

Form

capsule, delayed release, oral

Strength

20 mg

Approval

ANDA ANDA075576

On the market since

Oct 13, 2010

Package NDCs

49999-265-00 49999-265-01 49999-265-14 49999-265-15 49999-265-28 49999-265-30 49999-265-60 49999-265-90

Official label

DailyMed (National Library of Medicine), updated Dec 16, 2024

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