Drugplain

NDC 31722-895-30

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 (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 blood pressure in patients with hypertension.

Key Facts

Brand Name
Olmesartan medoxomil, amlodipine and hydrochlorothiazide
Generic Name
Olmesartan medoxomil, amlodipine and hydrochlorothiazide
NDC Code (Package)
31722-895-30
NDC Code (Product)
31722-895
Manufacturer
Camber Pharmaceuticals, Inc.
Strength
10 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA209242
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
10/06/2025

Recall History

No Recall History

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