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Cyclosporine - 54868-5522-0 - (Cyclosporine)

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Drug Information of Cyclosporine

Product NDC: 54868-5522
Proprietary Name: Cyclosporine
Non Proprietary Name: Cyclosporine
Active Ingredient(s): 100    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: 54868-5522
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065040
Marketing Category: ANDA
Start Marketing Date: 20060210

Package Information of Cyclosporine

Package NDC: 54868-5522-0
Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-5522-0)

NDC Information of Cyclosporine

NDC Code 54868-5522-0
Proprietary Name Cyclosporine
Package Description 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-5522-0)
Product NDC 54868-5522
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclosporine
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20060210
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CYCLOSPORINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA]

Complete Information of Cyclosporine


General Information