Finasteride

Product NDC

67046-695

11-digit product format

670460695

Labeler code

67046

Product ID

67046-695_68a7e4c2-bcb5-b8fd-e053-2a91aa0a2182

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Finasteride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Contract Pharmacy Services-PA

Application

ANDA090121

Marketing category

ANDA

Marketing start

2018-03-30

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