NDC 65862-741 – Olmesartan Medoxomil

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

Human Prescription Drug

Product NDC65862-741

Product details

Brand name
Olmesartan Medoxomil
Generic name
Olmesartan Medoxomil
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204798
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
65862-741-01100 TABLET, FILM COATED in 1 BOTTLE (65862-741-01)Apr 24, 2017
65862-741-05500 TABLET, FILM COATED in 1 BOTTLE (65862-741-05)Apr 24, 2017
65862-741-3030 TABLET, FILM COATED in 1 BOTTLE (65862-741-30)Apr 24, 2017
65862-741-9090 TABLET, FILM COATED in 1 BOTTLE (65862-741-90)Apr 24, 2017

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