Lisinopril

Product NDC

53808-0702

11-digit product format

538080702

Labeler code

53808

Product ID

53808-0702_68a98d1d-a74f-4d43-9ebe-c50795b3975b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lisinopril

Dosage form

TABLET

Route

ORAL

Labeler

State of Florida DOH Central Pharmacy

Application

ANDA076071

Marketing category

ANDA

Marketing start

2009-07-01

Marketing end

0000-00-00

Substance

LISINOPRIL

Active strength

20 mg/1

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record