Drugplain

NDC 71335-2180-2

Olmesartan Medoxomil and Hydrochlorothiazide 12.5 mg/1

Olmesartan Medoxomil and Hydrochlorothiazide · TABLET

No Recall History

Olmesartan Medoxomil and Hydrochlorothiazide is a tablet containing olmesartan medoxomil and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by Bryant Ranch Prepack.

Key Facts

Brand Name
Olmesartan Medoxomil and Hydrochlorothiazide
Generic Name
Olmesartan Medoxomil and Hydrochlorothiazide
NDC Code (Package)
71335-2180-2
NDC Code (Product)
71335-2180
Manufacturer
Bryant Ranch Prepack
Strength
12.5 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA208847
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
10/01/2020

Recall History

No Recall History

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