Finasteride

Product NDC

50436-0455

11-digit product format

504360455

Labeler code

50436

Product ID

50436-0455_64d363d9-3dc1-4166-b0fc-699eb12eaca7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Finasteride

Dosage form

TABLET, COATED

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA207750

Marketing category

ANDA

Marketing start

2017-01-06

Marketing end

0000-00-00

Substance

FINASTERIDE

Active strength

1 mg/1

Pharmacologic classes

5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record