Losartan Potassium and Hydrochlorothiazide

Product NDC

55700-059

11-digit product format

557000059

Labeler code

55700

Product ID

55700-059_4826b8ee-0d1b-4263-b3a2-0715097ed183

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA090528

Marketing category

ANDA

Marketing start

2010-10-06

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM

Active strength

13 mg/1; mg/1

Pharmacologic classes

Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],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