NDC 73190-080 – Olmesartan medoxomil-hydrochlorothiazide

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

Human Prescription Drug

Product NDC73190-080

Product details

Brand name
Olmesartan medoxomil-hydrochlorothiazide
Generic name
Olmesartan medoxomil-hydrochlorothiazide
Labeler
AvKARE
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA021532
Marketed since
July 14, 2026
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Olmesartan medoxomil-hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
73190-080-9090 TABLET, FILM COATED in 1 BOTTLE (73190-080-90)Jul 14, 2026

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