Class II · Moderate risk
Amoxicillin Capsules
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0781-2613-05 recalled?
Amoxicillin · 500 CAPSULE in 1 BOTTLE (0781-2613-05)
Yes — this exact package was recalled
1 FDA recall names the code 0781-2613-05 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
- Amoxicillin
- Strength
- AMOXICILLIN 500 mg/1
- Form
- Capsule · Oral
- Labeler
- Sandoz Inc
- Type
- Human Prescription Drug
- Product code
- 0781-2613
Recalls naming this package
Class II · Moderate risk
Amoxicillin Capsules USP 500 mg
Presence of Foreign Substance, Sandoz is recalling certain lots of Amoxicillin Capsules, USP 500 mg due to potential contamination with fragments of stainless steel wire mesh.
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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