NDC 71335-2448 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC71335-2448

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 (4)

Package NDCDescriptionSince
71335-2448-130 TABLET, COATED in 1 BOTTLE (71335-2448-1)Aug 15, 2024
71335-2448-260 TABLET, COATED in 1 BOTTLE (71335-2448-2)Aug 15, 2024
71335-2448-390 TABLET, COATED in 1 BOTTLE (71335-2448-3)Aug 15, 2024
71335-2448-4180 TABLET, COATED in 1 BOTTLE (71335-2448-4)Aug 15, 2024

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