NDC 50090-3701 – Olmesartan Medoxomil and Hydrochlorothiazide

Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-3701

Product details

Brand name
Olmesartan Medoxomil and Hydrochlorothiazide
Generic name
Olmesartan Medoxomil and Hydrochlorothiazide
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205391
Marketed since
April 24, 2017
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →

Package NDC codes (2)

Package NDCDescriptionSince
50090-3701-030 TABLET, FILM COATED in 1 BOTTLE (50090-3701-0)Oct 9, 2019
50090-3701-190 TABLET, FILM COATED in 1 BOTTLE (50090-3701-1)Oct 22, 2018

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