Class II ยท Moderate risk
Amlodipine and Olmesartan Medoxomil Tablets
Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications
National Drug Code
Is NDC 67877-0500-30 recalled?
Amlodipine and olmesartan Medoxomil · 30 TABLET in 1 BOTTLE (67877-500-30)
Yes — this exact package was recalled
1 FDA recall names the code 67877-0500-30 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.
1 of these recalls is still ongoing.
- Active ingredient
- Amlodipine and olmesartan Medoxomil
- Strength
- AMLODIPINE BESYLATE 10 mg/1; OLMESARTAN MEDOXOMIL 20 mg/1
- Form
- Tablet · Oral
- Labeler
- Ascend Laboratories, LLC
- Type
- Human Prescription Drug
- Product code
- 67877-0500
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
- 67877-0545 Cephalexin 4
- 67877-0544 Cephalexin 3
- 67877-0590 Metoprolol Succinate 3
- 67877-0446 Olmesartan Medoxomil 2
- 67877-0474 Dabigatran Etexilate 2
- 67877-0475 Dabigatran Etexilate 2
Free recall alerts
Know the day your medication is recalled
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