Finasteride

Product NDC

0378-5036

11-digit product format

003785036

Labeler code

0378

Product ID

0378-5036_2a19c2f1-4dbf-48ac-a163-b97cf915c447

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA077578

Marketing category

ANDA

Marketing start

2015-10-20

Marketing end

2019-06-30

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