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Cyclosporine - 55390-122-10 - (Cyclosporine)

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Drug Information of Cyclosporine

Product NDC: 55390-122
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: 55390-122
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065004
Marketing Category: ANDA
Start Marketing Date: 19991215

Package Information of Cyclosporine

Package NDC: 55390-122-10
Package Description: 10 VIAL in 1 BOX (55390-122-10) > 5 mL in 1 VIAL

NDC Information of Cyclosporine

NDC Code 55390-122-10
Proprietary Name Cyclosporine
Package Description 10 VIAL in 1 BOX (55390-122-10) > 5 mL in 1 VIAL
Product NDC 55390-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclosporine
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19991215
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name CYCLOSPORINE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA]

Complete Information of Cyclosporine


General Information