NDC 63629-4307 – Olmesartan Medoxomil and Hydrochlorothiazide

Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-4307

Product details

Brand name
Olmesartan Medoxomil and Hydrochlorothiazide
Generic name
Olmesartan Medoxomil and Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204233
Marketed since
April 24, 2017
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
63629-4307-190 TABLET in 1 BOTTLE (63629-4307-1)Jun 26, 2024

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