NDC 70518-4165 – 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 NDC70518-4165

Product details

Brand name
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Generic name
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206137
Marketed since
August 22, 2024
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 (1)

Package NDCDescriptionSince
70518-4165-030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4165-0)Aug 22, 2024

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