Losartan Potassium and Hydrochlorothiazide

Product NDC

70518-0354

11-digit product format

705180354

Labeler code

70518

Product ID

70518-0354_83d74b52-a18f-5664-e053-2a91aa0a9bfd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Losartan Potassium and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA090528

Marketing category

ANDA

Marketing start

2017-03-23

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM

Active strength

25 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