Drugplain

NDC 63629-2240-1

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 10 mg/1

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide · TABLET, FILM COATED

No Recall History

This is a combination blood pressure medication that contains three active ingredients: olmesartan (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 besylate / hydrochlorothiazide
Generic Name
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
NDC Code (Package)
63629-2240-1
NDC Code (Product)
63629-2240
Manufacturer
Bryant Ranch Prepack
Strength
10 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA206137
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
10/26/2016

Recall History

No Recall History

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