Losartan Potassium

Product NDC

68788-6462

11-digit product format

687886462

Labeler code

68788

Product ID

68788-6462_3e218094-c751-42b8-9b40-2413a6748f5d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

losartan potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc

Application

ANDA091497

Marketing category

ANDA

Marketing start

2016-08-15

Marketing end

0000-00-00

Substance

LOSARTAN POTASSIUM

Active strength

100 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record