"42385-922-37" National Drug Code (NDC)

NDC Code	42385-922-37
Package Description	5 BLISTER PACK in 1 CARTON (42385-922-37) / 6 CAPSULE in 1 BLISTER PACK (42385-922-06)
Product NDC	42385-922
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Atazanavir
Non-Proprietary Name	Atazanavir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20210430
Marketing Category Name	ANDA
Application Number	ANDA212579
Manufacturer	Laurus Labs Limited
Substance Name	ATAZANAVIR SULFATE
Strength	300
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], HIV Protease Inhibitors [MoA], Protease Inhibitor [EPC], UDP Glucuronosyltransferases Inhibitors [MoA], UGT1A1 Inhibitors [MoA]