Losartan Potassium

Product NDC

0615-7605

11-digit product format

006157605

Labeler code

0615

Product ID

0615-7605_21e68075-8d82-4bd8-be9c-05ef2647dc20

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA076958

Marketing category

ANDA

Marketing start

2010-04-06

Marketing end

0000-00-00

Substance

LOSARTAN POTASSIUM

Active strength

50 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record