NDC 70934-479
Omeprazole 20 mg capsule, delayed release
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. 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 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.
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
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
- Strength
- 20 mg
- Approval
- ANDA ANDA075410
- On the market since
- Dec 31, 2019
- Package NDCs
70934-479-6070934-479-90- 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?