"0172-7312-46" National Drug Code (NDC)

NDC Code	0172-7312-46
Package Description	30 BLISTER PACK in 1 CARTON (0172-7312-46) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0172-7312-00)
Product NDC	0172-7312
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Cyclosporine
Proprietary Name Suffix	Modified
Non-Proprietary Name	Cyclosporine
Dosage Form	CAPSULE, LIQUID FILLED
Usage	ORAL
Start Marketing Date	20050329
End Marketing Date	20170331
Marketing Category Name	ANDA
Application Number	ANDA065110
Manufacturer	IVAX Pharmaceuticals, Inc.
Substance Name	CYCLOSPORINE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]