Lisinopril

Product NDC

70518-0575

11-digit product format

705180575

Labeler code

70518

Product ID

70518-0575_860daee0-aafc-730d-e053-2a91aa0acb55

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

lisinopril

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076071

Marketing category

ANDA

Marketing start

2017-06-14

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

2020-12-31

Current FDA listing

Historical FDA.report record