Losartan Potassium

Product NDC

68788-6405

11-digit product format

687886405

Labeler code

68788

Product ID

68788-6405_bc6ded3a-3f71-44c4-8094-e2e8f5c840d9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA203835

Marketing category

ANDA

Marketing start

2016-06-09

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