Losartan Potassium

Product NDC

50268-517

11-digit product format

502680517

Labeler code

50268

Product ID

50268-517_9c96eb16-1576-ed74-e053-2a95a90a11bc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA090467

Marketing category

ANDA

Marketing start

2014-04-04

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

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record