Olmesartan Medoxomil

Product NDC

42292-036

11-digit product format

422920036

Labeler code

42292

Product ID

42292-036_7d631f39-5284-1814-e053-2991aa0a92ed

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

olmesartan medoxomil

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA078276

Marketing category

ANDA

Marketing start

2016-11-10

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