lisinopril

Product NDC

50436-7988

11-digit product format

504367988

Labeler code

50436

Product ID

50436-7988_cdee60e6-2470-44ae-bb67-ff45584ce80d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lisinopril

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA075994

Marketing category

ANDA

Marketing start

2002-07-01

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record