Naftifine Hydrochloride

Product NDC

40085-201

11-digit product format

400850201

Labeler code

40085

Product ID

40085-201_00484c06-4cd0-4788-a4ce-1e21e50d6ae3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

NAFTIFINE HYDROCHLORIDE

Dosage form

CREAM

Route

TOPICAL

Labeler

Renaissance Pharma, Inc.

Application

NDA019599

Marketing category

NDA

Marketing start

2016-10-01

Marketing end

2020-04-30

Substance

NAFTIFINE HYDROCHLORIDE

Active strength

1 mg/g

Pharmacologic classes

Allylamine [CS],Allylamine Antifungal [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record