NDC 50090-3471 – Olmesartan medoxomil

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

Human Prescription Drug

Product NDC50090-3471

Product details

Brand name
Olmesartan medoxomil
Generic name
Olmesartan medoxomil
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207662
Marketed since
April 27, 2017
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
50090-3471-030 TABLET, FILM COATED in 1 BOTTLE (50090-3471-0)Jan 31, 2019
50090-3471-190 TABLET, FILM COATED in 1 BOTTLE (50090-3471-1)Jun 11, 2018

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