Home
>
National Drug Code (NDC)
>
Ketoconazole
Ketoconazole - 21695-562-30 - (Ketoconazole)
Drug Information of Ketoconazole
| Product NDC: | 21695-562 |
| Proprietary Name: | Ketoconazole |
| Non Proprietary Name: | Ketoconazole |
| Active Ingredient(s): | 200 mg/1 & nbsp; Ketoconazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketoconazole
| Product NDC: | 21695-562 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075319 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990615 |
Package Information of Ketoconazole
| Package NDC: | 21695-562-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (21695-562-30) |
NDC Information of Ketoconazole
| NDC Code | 21695-562-30 |
| Proprietary Name | Ketoconazole |
| Package Description | 30 TABLET in 1 BOTTLE (21695-562-30) |
| Product NDC | 21695-562 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ketoconazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990615 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | KETOCONAZOLE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
