NDC 70756-813 – Olmesartan Medoxomil and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC70756-813

Product details

Brand name
Olmesartan Medoxomil and Hydrochlorothiazide
Generic name
Olmesartan Medoxomil and Hydrochlorothiazide
Labeler
Lifestar Pharma LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208847
Marketed since
October 1, 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 (4)

Package NDCDescriptionSince
70756-813-121000 TABLET in 1 BOTTLE (70756-813-12)Oct 1, 2020
70756-813-3030 TABLET in 1 BOTTLE (70756-813-30)Oct 1, 2020
70756-813-51500 TABLET in 1 BOTTLE (70756-813-51)Oct 1, 2020
70756-813-9090 TABLET in 1 BOTTLE (70756-813-90)Oct 1, 2020

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