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LAMISIL AT
LAMISIL AT - 0067-4000-01 - (TERBINAFINE HYDROCHLORIDE)
Drug Information of LAMISIL AT
| Product NDC: | 0067-4000 |
| Proprietary Name: | LAMISIL AT |
| Non Proprietary Name: | TERBINAFINE HYDROCHLORIDE |
| Active Ingredient(s): | 1 mL/100mL & nbsp; TERBINAFINE HYDROCHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LAMISIL AT
| Product NDC: | 0067-4000 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021124 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000501 |
Package Information of LAMISIL AT
| Package NDC: | 0067-4000-01 |
| Package Description: | 30 mL in 1 BOTTLE, PUMP (0067-4000-01) |
NDC Information of LAMISIL AT
| NDC Code | 0067-4000-01 |
| Proprietary Name | LAMISIL AT |
| Package Description | 30 mL in 1 BOTTLE, PUMP (0067-4000-01) |
| Product NDC | 0067-4000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TERBINAFINE HYDROCHLORIDE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20000501 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | TERBINAFINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
