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CYCLOSPORINE
CYCLOSPORINE - 62584-827-21 - (CYCLOSPORINE)
Drug Information of CYCLOSPORINE
| Product NDC: | 62584-827 |
| Proprietary Name: | CYCLOSPORINE |
| Non Proprietary Name: | CYCLOSPORINE |
| Active Ingredient(s): | 100 mg/1 & nbsp; CYCLOSPORINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CYCLOSPORINE
| Product NDC: | 62584-827 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065040 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091211 |
Package Information of CYCLOSPORINE
| Package NDC: | 62584-827-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (62584-827-21) > 30 CAPSULE in 1 BLISTER PACK (62584-827-11) |
NDC Information of CYCLOSPORINE
| NDC Code | 62584-827-21 |
| Proprietary Name | CYCLOSPORINE |
| Package Description | 3 BLISTER PACK in 1 CARTON (62584-827-21) > 30 CAPSULE in 1 BLISTER PACK (62584-827-11) |
| Product NDC | 62584-827 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CYCLOSPORINE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20091211 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | CYCLOSPORINE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA] |
