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Cyclosporine - 60505-0134-1 - (Cyclosporine)

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Drug Information of Cyclosporine

Product NDC: 60505-0134
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: 60505-0134
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065040
Marketing Category: ANDA
Start Marketing Date: 20020529

Package Information of Cyclosporine

Package NDC: 60505-0134-1
Package Description: 1000 CAPSULE, LIQUID FILLED in 1 BOTTLE (60505-0134-1)

NDC Information of Cyclosporine

NDC Code 60505-0134-1
Proprietary Name Cyclosporine
Package Description 1000 CAPSULE, LIQUID FILLED in 1 BOTTLE (60505-0134-1)
Product NDC 60505-0134
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclosporine
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20020529
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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