lisinopril

Product NDC

68001-269

11-digit product format

680010269

Labeler code

68001

Product ID

68001-269_9494cf39-52ea-496c-89ac-5915bb2f0d8b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lisinopril

Dosage form

TABLET

Route

ORAL

Labeler

BluePoint Laboratories

Application

ANDA075994

Marketing category

ANDA

Marketing start

2015-07-06

Marketing end

2019-10-31

Substance

LISINOPRIL

Active strength

20 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record