Olmesartan Medoxomil and Hydrochlorothiazide

Product NDC

0093-7615

11-digit product format

000937615

Labeler code

0093

Product ID

0093-7615_b0b475ff-035d-42e8-b43a-92c9ed320cf6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Olmesartan Medoxomil and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

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

2020-12-31

Current FDA listing

Historical FDA.report record