Dutasteride

Product NDC

50090-2285

11-digit product format

500902285

Labeler code

50090

Product ID

50090-2285_65fbadbc-704d-4235-b1f3-05427dbaf13f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

dutasteride

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA204292

Marketing category

ANDA

Marketing start

2015-11-25

Marketing end

0000-00-00

Substance

DUTASTERIDE

Active strength

1 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