Losartan Potassium

Product NDC

68071-3014

11-digit product format

680713014

Labeler code

68071

Product ID

68071-3014_4ab5378e-cce8-1f64-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA091497

Marketing category

ANDA

Marketing start

2014-07-30

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

2019-12-31

Current FDA listing

Historical FDA.report record