Losartan Potassium and Hydrochlorothiazide

Product NDC

50268-514

11-digit product format

502680514

Labeler code

50268

Product ID

50268-514_81695f4d-b9a5-691e-e053-2991aa0a5d63

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA090528

Marketing category

ANDA

Marketing start

2014-04-14

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

2020-12-31

Current FDA listing

Historical FDA.report record