Home
>
National Drug Code (NDC)
>
CLOTRIMAZOLE
CLOTRIMAZOLE - 16590-060-30 - (CLOTRIMAZOLE)
Drug Information of CLOTRIMAZOLE
| Product NDC: | 16590-060 |
| 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: | 16590-060 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072640 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930831 |
Package Information of CLOTRIMAZOLE
| Package NDC: | 16590-060-30 |
| Package Description: | 30 g in 1 TUBE (16590-060-30) |
NDC Information of CLOTRIMAZOLE
| NDC Code | 16590-060-30 |
| Proprietary Name | CLOTRIMAZOLE |
| Package Description | 30 g in 1 TUBE (16590-060-30) |
| Product NDC | 16590-060 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CLOTRIMAZOLE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19930831 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
