Losartan Potassium

Product NDC

63629-6381

11-digit product format

636296381

Labeler code

63629

Product ID

63629-6381_5bd44386-4017-4580-a2be-35607c488ce3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076958

Marketing category

ANDA

Marketing start

2010-04-06

Marketing end

0000-00-00

Substance

LOSARTAN POTASSIUM

Active strength

25 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