NDC 50090-7127 – OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-7127

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 · ANDA207804
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 (1)

Package NDCDescriptionSince
50090-7127-090 TABLET in 1 BOTTLE (50090-7127-0)Apr 9, 2024

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