Lamisil

Product NDC

0078-0179

11-digit product format

000780179

Labeler code

0078

Product ID

0078-0179_36c4239e-e209-4091-aa18-ecc988249aac

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

terbinafine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Novartis Pharmaceuticals

Application

NDA020539

Marketing category

NDA

Marketing start

1996-05-10

Marketing end

0000-00-00

Substance

TERBINAFINE HYD

Active strength

250 mg/1

Pharmacologic classes

Allylamine [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record