NDC 71335-2399 – Olmesartan Medoxomil

Olmesartan Medoxomil 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2399

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan medoxomil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206720
Marketed since
March 4, 2022
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
71335-2399-130 TABLET in 1 BOTTLE (71335-2399-1)Jun 13, 2024
71335-2399-260 TABLET in 1 BOTTLE (71335-2399-2)Jun 13, 2024
71335-2399-390 TABLET in 1 BOTTLE (71335-2399-3)Jun 13, 2024
71335-2399-4180 TABLET in 1 BOTTLE (71335-2399-4)Jun 13, 2024

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