NDC 46708-132 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC46708-132

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203012
Marketed since
April 24, 2017
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 (4)

Package NDCDescriptionSince
46708-132-10100 TABLET, FILM COATED in 1 CARTON (46708-132-10)Apr 24, 2017
46708-132-3030 TABLET, FILM COATED in 1 BOTTLE (46708-132-30)Apr 24, 2017
46708-132-9090 TABLET, FILM COATED in 1 BOTTLE (46708-132-90)Apr 24, 2017
46708-132-911000 TABLET, FILM COATED in 1 BOTTLE (46708-132-91)Apr 24, 2017

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