Class III · Low risk
Olmesartan Medoxomil Tablets
Presence of Foreign Tablet/Capsule
National Drug Code
Is NDC 67877-0446-90 recalled?
Olmesartan Medoxomil · 90 TABLET, COATED in 1 BOTTLE (67877-446-90)
Yes — this exact package was recalled
1 FDA recall names the code 67877-0446-90 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
- Olmesartan Medoxomil
- Strength
- OLMESARTAN MEDOXOMIL 20 mg/1
- Form
- Tablet, Coated · Oral
- Labeler
- Ascend Laboratories, LLC
- Type
- Human Prescription Drug
- Product code
- 67877-0446
Recalls naming this package
Class II · Moderate risk
Olmesartan Medoxomil Tablets 20 mg
cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error with alternate API source prior to filing and approval of Prior Approval Supplement.
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
- 67877-0474 Dabigatran Etexilate 2
- 67877-0475 Dabigatran Etexilate 2
- 67877-0501 Amlodipine and olmesartan Medoxomil 2
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