Lisinopril

Product NDC

53808-0868

11-digit product format

538080868

Labeler code

53808

Product ID

53808-0868_5584341f-746e-4791-a1fa-36b5e8c865d1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril

Dosage form

TABLET

Route

ORAL

Labeler

State of Florida DOH Central Pharmacy

Application

ANDA076059

Marketing category

ANDA

Marketing start

2013-01-01

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