Product NDC: | 0067-6293 |
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): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0067-6293 |
Labeler Name: | Novartis Consumer Health, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021124 |
Marketing Category: | NDA |
Start Marketing Date: | 20090723 |
Package NDC: | 0067-6293-83 |
Package Description: | 125 mL in 1 BOTTLE, SPRAY (0067-6293-83) |
NDC Code | 0067-6293-83 |
Proprietary Name | LAMISIL |
Package Description | 125 mL in 1 BOTTLE, SPRAY (0067-6293-83) |
Product NDC | 0067-6293 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TERBINAFINE HYDROCHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20090723 |
Marketing Category Name | NDA |
Labeler Name | Novartis Consumer Health, Inc. |
Substance Name | TERBINAFINE HYDROCHLORIDE |
Strength Number | 1.25 |
Strength Unit | mL/125mL |
Pharmaceutical Classes |