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Clotrimazole
Clotrimazole - 21695-935-45 - (Clotrimazole)
Drug Information of Clotrimazole
| Product NDC: | 21695-935 |
| Proprietary Name: | Clotrimazole |
| Non Proprietary Name: | Clotrimazole |
| Active Ingredient(s): | 50 mg/g & nbsp; Clotrimazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clotrimazole
| Product NDC: | 21695-935 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074165 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930716 |
Package Information of Clotrimazole
| Package NDC: | 21695-935-45 |
| Package Description: | 45 g in 1 TUBE (21695-935-45) |
NDC Information of Clotrimazole
| NDC Code | 21695-935-45 |
| Proprietary Name | Clotrimazole |
| Package Description | 45 g in 1 TUBE (21695-935-45) |
| Product NDC | 21695-935 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19930716 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
