Class III ยท Low risk
Amoxicillin for Oral Suspension
Discoloration: This recall is being carried out due to an orange to brown discolored Amoxicillin powder on the inner foil seal of the bottles. This is an expansion of RES 65050.
National Drug Code
Is NDC 0093-4160-78 recalled?
Amoxicillin · 75 mL in 1 BOTTLE (0093-4160-78)
Yes — this exact package was recalled
1 FDA recall names the code 0093-4160-78 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 200 mg/5mL
- Form
- Powder, for Suspension · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-4160
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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