NDC 68071-5044
Omeprazole 20 mg capsule, delayed release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.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 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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels 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
- Nov 4, 2002
- Package NDCs
68071-5044-3- Official label
- DailyMed (National Library of Medicine), updated Feb 19, 2021
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