Finasteride

Product NDC

55154-4396

11-digit product format

551544396

Labeler code

55154

Product ID

55154-4396_a9926458-44e3-42a4-bc0e-8be5dd0d28b8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA077578

Marketing category

ANDA

Marketing start

2015-07-13

Marketing end

0000-00-00

Substance

FINASTERIDE

Active strength

5 mg/1

Pharmacologic classes

5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record