Finasteride

Product NDC

50268-323

11-digit product format

502680323

Labeler code

50268

Product ID

50268-323_9c966244-3ea9-150c-e053-2995a90acaf0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvPAK

Application

ANDA077914

Marketing category

ANDA

Marketing start

2011-03-21

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