Omeprazole 40 mg capsule, delayed release

Where it's made

This label doesn't name the factory that makes the drug (it lists 1 site that packages it and labels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lannett Company, Inc. names for other drugs.

Recalls

• Sep 16, 2013 · Class II · Kremers Urban Pharmaceuticals, Inc.
  Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
  Lots: Lot Number 59627; Expiration Date 02/2014

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Omeprazole: every company that makes it

Form

capsule, delayed release, oral

Strength

40 mg

Approval

ANDA ANDA075410

On the market since

Jan 23, 2009

Package NDCs

62175-136-32 62175-136-37 62175-136-43 62175-136-46 62175-136-49

Official label

DailyMed (National Library of Medicine), updated Apr 21, 2023

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