FINASTERIDE

Product NDC

45963-600

11-digit product format

459630600

Labeler code

45963

Product ID

45963-600_d7f02177-8eae-44fe-8dd4-3f136b7c5b16

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

FINASTERIDE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA078371

Marketing category

ANDA

Marketing start

2013-11-05

Marketing end

0000-00-00

Substance

FINASTERIDE

Active strength

1 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