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Ketodan
Ketodan - 43538-531-10 - (ketoconazole)
Drug Information of Ketodan
| Product NDC: | 43538-531 |
| Proprietary Name: | Ketodan |
| Non Proprietary Name: | ketoconazole |
| Active Ingredient(s): | & nbsp; ketoconazole |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketodan
| Product NDC: | 43538-531 |
| Labeler Name: | Medimetriks Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091550 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120615 |
Package Information of Ketodan
| Package NDC: | 43538-531-10 |
| Package Description: | 1 KIT in 1 CARTON (43538-531-10) * 100 g in 1 CAN * 454 g in 1 BOTTLE, PUMP |
NDC Information of Ketodan
| NDC Code | 43538-531-10 |
| Proprietary Name | Ketodan |
| Package Description | 1 KIT in 1 CARTON (43538-531-10) * 100 g in 1 CAN * 454 g in 1 BOTTLE, PUMP |
| Product NDC | 43538-531 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ketoconazole |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120615 |
| Marketing Category Name | ANDA |
| Labeler Name | Medimetriks Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
