"70505-220-60" National Drug Code (NDC)

NDC Code	70505-220-60
Package Description	1 BOTTLE, PLASTIC in 1 CARTON (70505-220-60) / 60 CAPSULE in 1 BOTTLE, PLASTIC
Product NDC	70505-220
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nitisinone
Non-Proprietary Name	Nitisinone
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20230508
Marketing Category Name	ANDA
Application Number	ANDA212390
Manufacturer	Analog Pharma
Substance Name	NITISINONE
Strength	20
Strength Unit	mg/1
Pharmacy Classes	4-Hydroxyphenyl-Pyruvate Dioxygenase Inhibitor [EPC], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 2E1 Inducers [MoA], Hydroxyphenylpyruvate Dioxygenase Inhibitors [MoA], Organic Anion Transporter 1 Inhibitors [MoA], Organic Anion Transporter 3 Inhibitors [MoA]