NDC 70934-486

Omeprazole 40 mg capsule, delayed release

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's a repackaged product: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Lannett Company, Inc.'s NDC 62175-136.

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.

Repackaging site

• Denton Pharma, Inc. DBA Northwind Pharmaceuticals, · repackages it

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

Strength

40 mg

Approval

ANDA ANDA075410

On the market since

Jan 7, 2020

Package NDCs

70934-486-30 70934-486-60 70934-486-90

Official label

DailyMed (National Library of Medicine), updated Mar 19, 2020

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