NDC 70518-4165-0

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg/1

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

No Recall History

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide is a tablet, film coated containing olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide at a strength of 5 mg/1. Manufactured by REMEDYREPACK INC..

Key Facts

Brand Name: olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Generic Name: olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
NDC Code (Package): 70518-4165-0
NDC Code (Product): 70518-4165
Manufacturer: REMEDYREPACK INC.
Strength: 5 mg/1
Dosage Form: TABLET, FILM COATED
Route: ORAL
Marketing Status
Application #: ANDA206137
Drug Class: Thiazide Diuretic [EPC]
Marketing Start: 08/22/2024

Recall History

No Recall History

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