NDC 49884-788 – 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 NDC49884-788

Product details

Brand name
Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Generic name
Olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Labeler
Par Health USA, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206137
Marketed since
October 26, 2016
Listing expires
December 31, 2027
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 (2)

Package NDCDescriptionSince
49884-788-0990 TABLET, FILM COATED in 1 BOTTLE (49884-788-09)Oct 26, 2016
49884-788-1130 TABLET, FILM COATED in 1 BOTTLE (49884-788-11)Oct 26, 2016

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