Drugplain

NDC 67877-453-30

OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE 12.5 mg/1

OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE · TABLET, FILM COATED

No Recall History

OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE is a tablet, film coated containing olmesartan medoxomil and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by Ascend Laboratories, LLC.

Key Facts

Brand Name
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE
Generic Name
OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE
NDC Code (Package)
67877-453-30
NDC Code (Product)
67877-453
Manufacturer
Ascend Laboratories, LLC
Strength
12.5 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA207037
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
05/01/2025

Recall History

No Recall History

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