NDC 16729-320 – Olmesartan medoxomil

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

Human Prescription Drug

Product NDC16729-320

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
February 16, 2018
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
16729-320-1030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-320-10)Feb 16, 2018
16729-320-1590 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16729-320-15)Feb 16, 2018

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