Class II · Moderate risk
NEXIUM¿ (esomeprazole magnesium)
Presence of Foreign Tablets/Capsules: Confimed customer compliant by a retail pharmacist that an unopened bottle labeled as NEXIUM¿ capsules contained 60 SEROQUEL¿ XR tablets.
National Drug Code
Is NDC 0186-5020-31 recalled?
Nexium · 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-5020-31)
Yes — this exact package was recalled
1 FDA recall names the code 0186-5020-31 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
- Esomeprazole magnesium
- Strength
- ESOMEPRAZOLE MAGNESIUM TRIHYDRATE 20 mg/1
- Form
- Capsule, Delayed Release · Oral
- Labeler
- AstraZeneca Pharmaceuticals LP
- Type
- Human Prescription Drug
- Product code
- 0186-5020
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
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