olmesartan medoxomil

Product NDC

71335-1019

11-digit product format

713351019

Labeler code

71335

Product ID

71335-1019_74e5c51b-5822-4925-acc8-7bf233f9a445

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

olmesartan medoxomil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA205192

Marketing category

ANDA

Marketing start

2017-04-24

Marketing end

0000-00-00

Substance

OLMESARTAN MEDOXOMIL

Active strength

20 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record