Product NDC: | 49348-793 |
Proprietary Name: | Clotrimazole |
Non Proprietary Name: | Clotrimazole |
Active Ingredient(s): | 10 mg/g & nbsp; Clotrimazole |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-793 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074165 |
Marketing Category: | ANDA |
Start Marketing Date: | 19930719 |
Package NDC: | 49348-793-76 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (49348-793-76) > 45 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 49348-793-76 |
Proprietary Name | Clotrimazole |
Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (49348-793-76) > 45 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 49348-793 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Clotrimazole |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19930719 |
Marketing Category Name | ANDA |
Labeler Name | McKesson |
Substance Name | CLOTRIMAZOLE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes |