Class II ยท Moderate risk
Prilosec (Omeprazole Magnesium)
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 70515-0610-01 recalled?
Prilosec · 30 GRANULE, DELAYED RELEASE in 1 CARTON (70515-610-01)
Yes — this exact package was recalled
1 FDA recall names the code 70515-0610-01 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 magnesium
- Strength
- OMEPRAZOLE MAGNESIUM 10 mg/1
- Form
- Granule, Delayed Release · Oral
- Labeler
- Covis Pharma US, Inc
- Type
- Human Prescription Drug
- Product code
- 70515-0610
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.
Free recall alerts
Know the day your medication is recalled
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