NDC 50090-5450 – Olmesartan Medoxomil and Hydrochlorothiazide

Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-5450

Product details

Brand name
Olmesartan Medoxomil and Hydrochlorothiazide
Generic name
Olmesartan Medoxomil and Hydrochlorothiazide
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208847
Marketed since
October 1, 2020
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 (1)

Package NDCDescriptionSince
50090-5450-090 TABLET in 1 BOTTLE (50090-5450-0)Jan 25, 2021

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