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Cyclosporine - 0185-0933-30 - (Cyclosporine)

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Drug Information of Cyclosporine

Product NDC: 0185-0933
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: 0185-0933
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065017
Marketing Category: ANDA
Start Marketing Date: 20000113

Package Information of Cyclosporine

Package NDC: 0185-0933-30
Package Description: 30 BLISTER PACK in 1 CARTON (0185-0933-30) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Cyclosporine

NDC Code 0185-0933-30
Proprietary Name Cyclosporine
Package Description 30 BLISTER PACK in 1 CARTON (0185-0933-30) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 0185-0933
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclosporine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20000113
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name CYCLOSPORINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA]

Complete Information of Cyclosporine


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