Losartan Potassium

Product NDC

0781-5806

11-digit product format

007815806

Labeler code

0781

Product ID

0781-5806_ea4a85dd-1f98-48ee-98fe-1f4a09340cbd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

losartan potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc.

Application

NDA020386

Marketing category

NDA

Marketing start

1995-04-14

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

2018-12-31

Current FDA listing

Historical FDA.report record