Drugplain

NDC 0093-5003-56

Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 10 mg/1

Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide · TABLET, FILM COATED

No Recall History

This is a combination blood pressure medication containing three active ingredients: olmesartan medoxomil (an angiotensin II receptor blocker), amlodipine (a calcium channel blocker), and hydrochlorothiazide (a thiazide diuretic). It is taken by mouth as a tablet to help lower high blood pressure.

Key Facts

Brand Name
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
Generic Name
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
NDC Code (Package)
0093-5003-56
NDC Code (Product)
0093-5003
Manufacturer
Teva Pharmaceuticals USA, Inc.
Strength
10 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA202491
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
11/14/2016

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.