Losartan Potassium and Hydrochlorothiazide

Product NDC

70518-0602

11-digit product format

705180602

Labeler code

70518

Product ID

70518-0602_8641bb2d-60cc-fabd-e053-2a91aa0ab10c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077157

Marketing category

ANDA

Marketing start

2017-06-29

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record