NDC 67046-520

Omeprazole 20 mg capsule, delayed release pellets

On the label: Coupler Enterprises Inc.. It's a repackaged product: Coupler Enterprises Inc. rebottles it from Lannett Company, Inc.'s NDC 62175-118.

Where the pills inside were made

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

Recalls

• Sep 16, 2013 · Class II · Terminated
  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

Product details

Generic drug

Omeprazole: see every company that makes it

Form

capsule, delayed release pellets

Strength

20 mg

Approval

ANDA ANDA075410

On the market since

Mar 9, 2010

Package NDCs

67046-520-30 67046-520-60

Official label

DailyMed (National Library of Medicine), updated Mar 9, 2010

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