NDC 72189-549 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC72189-549

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204798
Marketed since
April 19, 2024
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
72189-549-3030 TABLET, FILM COATED in 1 BOTTLE (72189-549-30)Apr 19, 2024
72189-549-9090 TABLET, FILM COATED in 1 BOTTLE (72189-549-90)Apr 19, 2024

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