Class III · Low risk
Amlodipine and Olmesartan Medoxomil Tablets
Discoloration: This product is being recalled due to a confirmed pharmacist report that tablets from this lot were a pink color instead of cream (peach).
National Drug Code
Is NDC 65862-0855-30 recalled?
Amlodipine and Olmesartan Medoxomil · 30 TABLET, FILM COATED in 1 BOTTLE (65862-855-30)
Yes — this exact package was recalled
1 FDA recall names the code 65862-0855-30 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
- Amlodipine and Olmesartan Medoxomil
- Strength
- AMLODIPINE BESYLATE 5 mg/1; OLMESARTAN MEDOXOMIL 40 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Aurobindo Pharma Limited
- Type
- Human Prescription Drug
- Product code
- 65862-0855
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
- 65862-0053 Simvastatin 2
- 65862-0420 Sulfamethoxazole and Trimethoprim 2
- 65862-0573 Valsartan 2
- 65862-0739 Amlodipine and valsartan 2
- 65862-0840 Moxifloxacin 2
- 65862-0010 Metformin Hydrochloride 1
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