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