Lisinopril and Hydrochlorothiazide

Product NDC

57297-519

11-digit product format

572970519

Labeler code

57297

Product ID

57297-519_cb5ca667-3142-46d8-8537-c4510571eb22

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

LUPIN LIMITED

Application

ANDA077912

Marketing category

ANDA

Marketing start

2006-04-10

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE; LISINOPRIL

Active strength

13 mg/1; mg/1

Pharmacologic classes

Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record