Class II · Moderate risk
Ciprofloxacin Tablets USP
Presence of Foreign Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.
National Drug Code
Is NDC 0143-9928-01 recalled?
Ciprofloxacin · 100 TABLET, FILM COATED in 1 BOTTLE (0143-9928-01)
Yes — this exact package was recalled
1 FDA recall names the code 0143-9928-01 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
- Ciprofloxacin
- Strength
- CIPROFLOXACIN HYDROCHLORIDE 500 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0143-9928
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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