Olmesartan Medoxomil and Hydrochlorothiazide

Product NDC

50090-3053

11-digit product format

500903053

Labeler code

50090

Product ID

50090-3053_5fed5903-fbda-4b80-b647-d4a46b0dae70

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olmesartan Medoxomil and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA200532

Marketing category

ANDA

Marketing start

2017-04-24

Marketing end

0000-00-00

Substance

OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE

Active strength

20 mg/1; mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record