NDC 50090-5402 – Olmesartan Medoxomil And Hydrochlorothiazide

Olmesartan Medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-5402

Product details

Brand name
Olmesartan Medoxomil And Hydrochlorothiazide
Generic name
Olmesartan Medoxomil And Hydrochlorothiazide
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209281
Marketed since
September 3, 2020
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
50090-5402-090 TABLET, FILM COATED in 1 BOTTLE (50090-5402-0)Dec 8, 2020

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