Class II ยท Moderate risk
Cefdinir for Oral Suspension
Defective Container: This recall is being carried out due to the potential for improperly sealed bottles.
National Drug Code
Is NDC 0093-4136-73 recalled?
Cefdinir · 100 mL in 1 BOTTLE (0093-4136-73)
Yes — this exact package was recalled
1 FDA recall names the code 0093-4136-73 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
- Cefdinir
- Strength
- CEFDINIR MONOHYDRATE 125 mg/5mL
- Form
- Powder, for Suspension · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-4136
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
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.