Class II ยท Moderate risk
Edarbi (azilsartan medoxomil)
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 60631-0080-30 recalled?
Edarbi · 30 TABLET in 1 BOTTLE (60631-080-30)
Yes — this exact package was recalled
1 FDA recall names the code 60631-0080-30 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
- Azilsartan kamedoxomil
- Strength
- AZILSARTAN KAMEDOXOMIL 80 mg/1
- Form
- Tablet · Oral
- Labeler
- Azurity Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 60631-0080
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
- 60631-0412 Edarbyclor 1
- 60631-0425 Edarbyclor 1
Free recall alerts
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