Finasteride

Product NDC

68084-399

11-digit product format

680840399

Labeler code

68084

Product ID

68084-399_735236c9-d008-f8d2-e053-2991aa0a2e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA077914

Marketing category

ANDA

Marketing start

2012-01-24

Marketing end

2019-07-31

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

0000-00-00

Current FDA listing

Historical FDA.report record