| 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 |