Losartan Potassium and Hydrochlorothiazide

Product NDC

70518-0112

11-digit product format

705180112

Labeler code

70518

Product ID

70518-0112_9f4cc354-1287-74aa-e053-2a95a90acc56

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

2017-01-10

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

2021-12-31

Current FDA listing

Historical FDA.report record