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Lotrimin Ultra
Lotrimin Ultra - 11523-7154-1 - (Butenafine Hydrochloride)
Drug Information of Lotrimin Ultra
| Product NDC: | 11523-7154 |
| Proprietary Name: | Lotrimin Ultra |
| Non Proprietary Name: | Butenafine Hydrochloride |
| Active Ingredient(s): | 10 mg/g & nbsp; Butenafine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lotrimin Ultra
| Product NDC: | 11523-7154 |
| Labeler Name: | MSD Consumer Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021307 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930923 |
Package Information of Lotrimin Ultra
| Package NDC: | 11523-7154-1 |
| Package Description: | 1 TUBE in 1 CARTON (11523-7154-1) > 12 g in 1 TUBE |
NDC Information of Lotrimin Ultra
| NDC Code | 11523-7154-1 |
| Proprietary Name | Lotrimin Ultra |
| Package Description | 1 TUBE in 1 CARTON (11523-7154-1) > 12 g in 1 TUBE |
| Product NDC | 11523-7154 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Butenafine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19930923 |
| Marketing Category Name | NDA |
| Labeler Name | MSD Consumer Care, Inc. |
| Substance Name | BUTENAFINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
