Lisinopril

Product NDC

55289-696

11-digit product format

552890696

Labeler code

55289

Product ID

55289-696_7b202e8d-d760-bb40-e053-2991aa0a540a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Lisinopril

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

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