Class II ยท Moderate risk
Omeprazole Delayed-Release Capsules
Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
National Drug Code
Is NDC 62175-0118-43 recalled?
Omeprazole · 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-43)
Yes — this exact package was recalled
1 FDA recall names the code 62175-0118-43 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- omeprazole
- Strength
- OMEPRAZOLE 20 mg/1
- Form
- Capsule, Delayed Release · Oral
- Labeler
- Lannett Company, Inc.
- Type
- Human Prescription Drug
- Product code
- 62175-0118
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 62175-0180 See recall 2
- 62175-0322 Niacin 2
- 62175-0106 isosorbide mononitrate 1
- 62175-0107 isosorbide mononitrate 1
- 62175-0123 See recall 1
- 62175-0124 See recall 1
Free recall alerts
Know the day your medication is recalled
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