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Econazole Nitrate
Econazole Nitrate - 21695-892-15 - (Econazole Nitrate)
Drug Information of Econazole Nitrate
| Product NDC: | 21695-892 |
| Proprietary Name: | Econazole Nitrate |
| Non Proprietary Name: | Econazole Nitrate |
| Active Ingredient(s): | 10 mg/g & nbsp; Econazole Nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Econazole Nitrate
| Product NDC: | 21695-892 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076479 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040623 |
Package Information of Econazole Nitrate
| Package NDC: | 21695-892-15 |
| Package Description: | 15 g in 1 TUBE (21695-892-15) |
NDC Information of Econazole Nitrate
| NDC Code | 21695-892-15 |
| Proprietary Name | Econazole Nitrate |
| Package Description | 15 g in 1 TUBE (21695-892-15) |
| Product NDC | 21695-892 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Econazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20040623 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | ECONAZOLE NITRATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
