Lisinopril and Hydrochlorothiazide

Product NDC

50436-7000

11-digit product format

504367000

Labeler code

50436

Product ID

50436-7000_d6e4ff81-2bdc-4cd0-be12-10326ef0087f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril and Hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA077912

Marketing category

ANDA

Marketing start

2006-10-04

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record