Product NDC: | 0168-0133 |
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: | 0168-0133 |
Labeler Name: | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078338 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080902 |
Package NDC: | 0168-0133-30 |
Package Description: | 30 g in 1 TUBE (0168-0133-30) |
NDC Code | 0168-0133-30 |
Proprietary Name | Clotrimazole |
Package Description | 30 g in 1 TUBE (0168-0133-30) |
Product NDC | 0168-0133 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clotrimazole |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20080902 |
Marketing Category Name | ANDA |
Labeler Name | E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc. |
Substance Name | CLOTRIMAZOLE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |