NDC 16729-322 – Olmesartan medoxomil

Olmesartan Medoxomil 40 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC16729-322

Product details

Brand name
Olmesartan medoxomil
Generic name
Olmesartan medoxomil
Labeler
Accord Healthcare Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207662
Marketed since
April 27, 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 (3)

Package NDCDescriptionSince
16729-322-1030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-10)Apr 27, 2017
16729-322-1590 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-15)Apr 27, 2017
16729-322-171000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-322-17)Apr 27, 2017

Other Olmesartan Medoxomil products