NDC 72162-1515 – Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide

Olmesartan Medoxomil 40 mg/1; Amlodipine Besylate 5 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-1515

Product details

Brand name
Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Generic name
Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206137
Marketed since
October 26, 2016
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
72162-1515-330 TABLET, FILM COATED in 1 BOTTLE (72162-1515-3)Oct 26, 2016

Other Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide products