NDC 72189-137 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC72189-137

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
December 2, 2020
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
72189-137-3030 TABLET, FILM COATED in 1 BOTTLE (72189-137-30)Dec 2, 2020
72189-137-9090 TABLET, FILM COATED in 1 BOTTLE (72189-137-90)Dec 2, 2020

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