Lisinopril

Product NDC

50436-5000

11-digit product format

504365000

Labeler code

50436

Product ID

50436-5000_d2e876c3-3e89-4260-956a-388237ad09fd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA076063

Marketing category

ANDA

Marketing start

2002-07-01

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record