NDC 72189-373 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC72189-373

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207662
Marketed since
August 15, 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 (1)

Package NDCDescriptionSince
72189-373-9090 TABLET, FILM COATED in 1 BOTTLE (72189-373-90)Aug 15, 2022

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