NDC 72189-660 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC72189-660

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208130
Marketed since
February 6, 2026
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
72189-660-3030 TABLET, FILM COATED in 1 BOTTLE (72189-660-30)Feb 6, 2026
72189-660-9090 TABLET, FILM COATED in 1 BOTTLE (72189-660-90)Feb 6, 2026

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