NDC 72189-548 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC72189-548

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 (1)

Package NDCDescriptionSince
72189-548-9090 TABLET, FILM COATED in 1 BOTTLE (72189-548-90)Apr 19, 2024

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