Class II ยท Moderate risk
Omeprazole Delayed-release Capsules
Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
National Drug Code
Is NDC 82009-0022-10 recalled?
Omeprazole · 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-022-10)
Yes — this exact package was recalled
1 FDA recall names the code 82009-0022-10 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.
1 of these recalls is still ongoing.
- Active ingredient
- Omeprazole
- Strength
- OMEPRAZOLE 20 mg/1
- Form
- Capsule, Delayed Release · Oral
- Labeler
- Quallent Pharmaceuticals Health LLC
- Type
- Human Prescription Drug
- Product code
- 82009-0022
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
- 82009-0032 Duloxetine 2
- 82009-0030 Duloxetine 1
- 82009-0117 Metformin ER 500 mg 1
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