Finasteride

Product NDC

45963-500

11-digit product format

459630500

Labeler code

45963

Product ID

45963-500_f1b4f46f-3ef1-4ae3-9e18-0c5b9d7bccb6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA077914

Marketing category

ANDA

Marketing start

2007-03-28

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

2021-12-31

Current FDA listing

Historical FDA.report record