Naftin

Product NDC

54766-102

11-digit product format

547660102

Labeler code

54766

Product ID

54766-102_b722781e-f782-66f6-e053-2995a90a0d2c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Naftifine Hydrochloride

Dosage form

CREAM

Route

TOPICAL

Labeler

Sebela Pharmaceuticals Inc.

Application

NDA019599

Marketing category

NDA

Marketing start

2018-02-28

Marketing end

2021-01-31

Substance

NAFTIFINE HYDROCHLORIDE

Active strength

10 mg/2g

Pharmacologic classes

Allylamine [CS],Allylamine Antifungal [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record