NDC 50090-7680 – Olmesartan Medoxomil

Olmesartan Medoxomil 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-7680

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 · ANDA211049
Marketed since
March 5, 2019
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
50090-7680-030 TABLET, FILM COATED in 1 BOTTLE (50090-7680-0)Oct 9, 2025
50090-7680-190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7680-1)Oct 9, 2025

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