Losartan Potassium and Hydrochlorothiazide

Product NDC

63739-527

11-digit product format

637390527

Labeler code

63739

Product ID

63739-527_165e9b85-0a98-4574-95d1-a6706713b009

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA091629

Marketing category

ANDA

Marketing start

2010-10-06

Marketing end

0000-00-00

Substance

LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE

Active strength

50 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

2020-12-31

Current FDA listing

Historical FDA.report record