NDC 71335-2600 – Olmesartan Medoxomil

Olmesartan Medoxomil 5 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71335-2600

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA206763
Marketed since
April 24, 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 (1)

Package NDCDescriptionSince
71335-2600-190 TABLET, COATED in 1 BOTTLE (71335-2600-1)Jun 5, 2025

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