Finasteride

Product NDC

51079-321

11-digit product format

510790321

Labeler code

51079

Product ID

51079-321_7be989ec-8bd0-12ba-e053-2a91aa0ae23b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA077578

Marketing category

ANDA

Marketing start

2015-07-13

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