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Cyclosporine
Cyclosporine - 0574-0866-10 - (Cyclosporine)
Drug Information of Cyclosporine
| Product NDC: | 0574-0866 |
| Proprietary Name: | Cyclosporine |
| Non Proprietary Name: | Cyclosporine |
| Active Ingredient(s): | 50 mg/mL & nbsp; Cyclosporine |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclosporine
| Product NDC: | 0574-0866 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065151 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031007 |
Package Information of Cyclosporine
| Package NDC: | 0574-0866-10 |
| Package Description: | 10 AMPULE in 1 CARTON (0574-0866-10) > 5 mL in 1 AMPULE |
NDC Information of Cyclosporine
| NDC Code | 0574-0866-10 |
| Proprietary Name | Cyclosporine |
| Package Description | 10 AMPULE in 1 CARTON (0574-0866-10) > 5 mL in 1 AMPULE |
| Product NDC | 0574-0866 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclosporine |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20031007 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | CYCLOSPORINE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA] |
