NDC 33342-173 – OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

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

Human Prescription Drug

Product NDC33342-173

Product details

Brand name
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Generic name
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Labeler
Macleods Pharmaceuticals Limited
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 (4)

Package NDCDescriptionSince
33342-173-0730 TABLET, FILM COATED in 1 BOTTLE (33342-173-07)Jun 2, 2023
33342-173-1090 TABLET, FILM COATED in 1 BOTTLE (33342-173-10)Jun 2, 2023
33342-173-1210 BLISTER PACK in 1 CARTON (33342-173-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKJun 2, 2023
33342-173-441000 TABLET, FILM COATED in 1 BOTTLE (33342-173-44)Jun 2, 2023

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