Class II · Moderate risk
edarbyclor Azilsartan Medoxomil and Chlorthalidone Tablets 40…
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 60631-0412-30 recalled?
Edarbyclor · 30 TABLET in 1 BOTTLE (60631-412-30)
Yes — this exact package was recalled
1 FDA recall names the code 60631-0412-30 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 and chlorthalidone
- Strength
- AZILSARTAN KAMEDOXOMIL 40 mg/1; CHLORTHALIDONE 12.5 mg/1
- Form
- Tablet · Oral
- Labeler
- Azurity Pharmaceuticals, Inc. (formerly Arbor Pharmaceuticals)
- Type
- Human Prescription Drug
- Product code
- 60631-0412
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
- 60631-0080 Edarbi 1
- 60631-0425 Edarbyclor 1
Free recall alerts
Know the day your medication is recalled
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