Class II ยท Moderate risk
Fenofibrate Capsules
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 27241-0118-04 recalled?
Fenofibrate · 100 CAPSULE in 1 BOTTLE (27241-118-04)
Yes — this exact package was recalled
1 FDA recall names the code 27241-0118-04 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
- Fenofibrate
- Strength
- FENOFIBRATE 67 mg/1
- Form
- Capsule · Oral
- Labeler
- Ajanta Pharma USA Inc.
- Type
- Human Prescription Drug
- Product code
- 27241-0118
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
- 27241-0056 Aripiprazole 1
- 27241-0097 Duloxetine 1
- 27241-0098 Duloxetine 1
- 27241-0099 Duloxetine 1
- 27241-0120 Fenofibrate 1
- 27241-0255 Fluphenazine hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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