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Cyclosporine
Cyclosporine - 0172-7311-46 - (Cyclosporine)
Drug Information of Cyclosporine
| Product NDC: | 0172-7311 |
| Proprietary Name: | Cyclosporine |
| Non Proprietary Name: | Cyclosporine |
| Active Ingredient(s): | 50 mg/1 & nbsp; Cyclosporine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cyclosporine
| Product NDC: | 0172-7311 |
| Labeler Name: | IVAX Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065110 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050428 |
Package Information of Cyclosporine
| Package NDC: | 0172-7311-46 |
| Package Description: | 30 BLISTER PACK in 1 CARTON (0172-7311-46) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0172-7311-00) |
NDC Information of Cyclosporine
| NDC Code | 0172-7311-46 |
| Proprietary Name | Cyclosporine |
| Package Description | 30 BLISTER PACK in 1 CARTON (0172-7311-46) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0172-7311-00) |
| Product NDC | 0172-7311 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cyclosporine |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20050428 |
| Marketing Category Name | ANDA |
| Labeler Name | IVAX Pharmaceuticals, Inc. |
| Substance Name | CYCLOSPORINE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA] |
