NDC 43547-392 – OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

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

Human Prescription Drug

Product NDC43547-392

Product details

Brand name
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Generic name
olmesartan medoxomil and hydrochlorothiazide
Labeler
Solco Healthcare US, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207804
Marketed since
April 24, 2017
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
43547-392-0330 TABLET in 1 BOTTLE (43547-392-03)Apr 24, 2017
43547-392-0990 TABLET in 1 BOTTLE (43547-392-09)Apr 24, 2017
43547-392-111000 TABLET in 1 BOTTLE (43547-392-11)Apr 24, 2017

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