NDC 31722-853 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC31722-853

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205499
Marketed since
May 23, 2025
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
31722-853-3030 TABLET, FILM COATED in 1 BOTTLE (31722-853-30)May 23, 2025
31722-853-9090 TABLET, FILM COATED in 1 BOTTLE (31722-853-90)May 23, 2025

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