Class II · Moderate risk
Neomycin Sulfate Tablets
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
National Drug Code
Is NDC 0093-1177-01 recalled?
Neomycin Sulfate · 100 TABLET in 1 BOTTLE (0093-1177-01)
Yes — this exact package was recalled
2 FDA recalls name the code 0093-1177-01 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
- Neomycin Sulfate
- Strength
- NEOMYCIN SULFATE 500 mg/1
- Form
- Tablet · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-1177
Recalls naming this package
Class II · Moderate risk
Neomycin Sulf Tablets
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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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