Drugplain

NDC 42571-248-05

OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE 10 mg/1

Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide · TABLET, FILM COATED

No Recall History

OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE is a tablet, film coated containing olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide at a strength of 10 mg/1. Manufactured by Micro Labs Limited.

Key Facts

Brand Name
OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE
Generic Name
Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide
NDC Code (Package)
42571-248-05
NDC Code (Product)
42571-248
Manufacturer
Micro Labs Limited
Strength
10 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA207437
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
03/01/2026

Recall History

No Recall History

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