losartan potassium

Product NDC

68071-1912

11-digit product format

680711912

Labeler code

68071

Product ID

68071-1912_48c133d5-0a79-424b-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

2011-06-01

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