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Clotrimazole
Clotrimazole - 68462-181-35 - (Clotrimazole)
Drug Information of Clotrimazole
| Product NDC: | 68462-181 |
| 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) |
Labeler Information of Clotrimazole
| Product NDC: | 68462-181 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090219 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100804 |
Package Information of Clotrimazole
| Package NDC: | 68462-181-35 |
| Package Description: | 30 g in 1 TUBE (68462-181-35) |
NDC Information of Clotrimazole
| NDC Code | 68462-181-35 |
| Proprietary Name | Clotrimazole |
| Package Description | 30 g in 1 TUBE (68462-181-35) |
| Product NDC | 68462-181 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100804 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
