Lamisil - 54868-6105-0 - (Terbinafine Hydrochloride)

Alphabetical Index


Drug Information of Lamisil

Product NDC: 54868-6105
Proprietary Name: Lamisil
Non Proprietary Name: Terbinafine Hydrochloride
Active Ingredient(s): 1.25    mL/125mL & nbsp;   Terbinafine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Lamisil

Product NDC: 54868-6105
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021124
Marketing Category: NDA
Start Marketing Date: 20100413

Package Information of Lamisil

Package NDC: 54868-6105-0
Package Description: 125 mL in 1 BOTTLE, SPRAY (54868-6105-0)

NDC Information of Lamisil

NDC Code 54868-6105-0
Proprietary Name Lamisil
Package Description 125 mL in 1 BOTTLE, SPRAY (54868-6105-0)
Product NDC 54868-6105
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Terbinafine Hydrochloride
Dosage Form Name SPRAY
Route Name TOPICAL
Start Marketing Date 20100413
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name TERBINAFINE HYDROCHLORIDE
Strength Number 1.25
Strength Unit mL/125mL
Pharmaceutical Classes

Complete Information of Lamisil


General Information