Losartan Potassium

Product NDC

68071-1989

11-digit product format

680711989

Labeler code

68071

Product ID

68071-1989_48fbb654-bba5-73d9-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

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

2020-12-31

Current FDA listing

Historical FDA.report record