"55292-322-20" National Drug Code (NDC)

NDC Code	55292-322-20
Package Description	20 TABLET, COATED in 1 BLISTER PACK (55292-322-20)
Product NDC	55292-322
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Isturisa
Non-Proprietary Name	Osilodrostat
Dosage Form	TABLET, COATED
Usage	ORAL
Start Marketing Date	20200331
Marketing Category Name	NDA
Application Number	NDA212801
Manufacturer	Recordati Rare Diseases, Inc.
Substance Name	OSILODROSTAT PHOSPHATE
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Cortisol Synthesis Inhibitor [EPC], Cytochrome P450 11B1 Inhibitors [MoA], Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA]