Finasteride

Product NDC

68071-1710

11-digit product format

680711710

Labeler code

68071

Product ID

68071-1710_518c0b9e-33a0-0a48-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA078341

Marketing category

ANDA

Marketing start

2007-10-30

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

2019-12-31

Current FDA listing

Historical FDA.report record