Lisinopril

Product NDC

0615-7639

11-digit product format

006157639

Labeler code

0615

Product ID

0615-7639_35e2befc-faf9-486b-97d3-71f98e7e6982

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA078402

Marketing category

ANDA

Marketing start

2007-04-19

Marketing end

0000-00-00

Substance

LISINOPRIL

Active strength

3 mg/1

Pharmacologic classes

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