NDC 71335-2996 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC71335-2996

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan medoxomil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208659
Marketed since
October 7, 2024
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
71335-2996-190 TABLET, COATED in 1 BOTTLE (71335-2996-1)Feb 4, 2026
71335-2996-230 TABLET, COATED in 1 BOTTLE (71335-2996-2)Feb 4, 2026

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