losartan potassium and hydrochlorothiazide

Product NDC

0781-5817

11-digit product format

007815817

Labeler code

0781

Product ID

0781-5817_83c4f278-a699-41b6-b372-63072cdbc202

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

losartan potassium and hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc.

Application

NDA020387

Marketing category

NDA

Marketing start

1995-04-28

Marketing end

0000-00-00

Substance

LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE

Active strength

100 mg/1; mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record