Class II ยท Moderate risk
Amoxicillin and Clavulanate Potassium for Oral Suspension USP
Subpotent drug; Clavulanate Potassium component
National Drug Code
Is NDC 0093-2277-07 recalled?
Amoxicillin and Clavulanate Potassium
Yes — this exact package was recalled
1 FDA recall names the code 0093-2277-07 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
- Amoxicillin and Clavulanate Potassium
- Strength
- AMOXICILLIN 200 mg/5mL; CLAVULANATE POTASSIUM 28.5 mg/5mL
- Form
- Powder, for Suspension · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-2277
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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