Losartan Potassium and Hydrochlorothiazide

Product NDC

0054-0277

11-digit product format

000540277

Labeler code

0054

Product ID

0054-0277_92240f7c-3335-451d-809e-2f9033d1a7ce

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

West-Ward Pharmaceuticals Corp.

Application

ANDA077732

Marketing category

ANDA

Marketing start

2010-04-06

Marketing end

2019-07-05

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

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record