NDC 50090-7478 – OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-7478

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 · ANDA204801
Marketed since
June 2, 2023
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 (2)

Package NDCDescriptionSince
50090-7478-030 TABLET, FILM COATED in 1 BOTTLE (50090-7478-0)Dec 19, 2024
50090-7478-190 TABLET, FILM COATED in 1 BOTTLE (50090-7478-1)Dec 19, 2024

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