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LAMISL AF
LAMISL AF - 0067-6266-30 - (Tolnaftate)
Drug Information of LAMISL AF
| Product NDC: | 0067-6266 |
| Proprietary Name: | LAMISL AF |
| Non Proprietary Name: | Tolnaftate |
| Active Ingredient(s): | 10 mg/g & nbsp; Tolnaftate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LAMISL AF
| Product NDC: | 0067-6266 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
Package Information of LAMISL AF
| Package NDC: | 0067-6266-30 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (0067-6266-30) > 30 g in 1 BOTTLE, SPRAY |
NDC Information of LAMISL AF
| NDC Code | 0067-6266-30 |
| Proprietary Name | LAMISL AF |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (0067-6266-30) > 30 g in 1 BOTTLE, SPRAY |
| Product NDC | 0067-6266 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tolnaftate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
