Losartan Potassium

Product NDC

68071-3102

11-digit product format

680713102

Labeler code

68071

Product ID

68071-3102_4aa21e89-b1fe-41b7-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA090467

Marketing category

ANDA

Marketing start

2010-10-06

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