"70771-1592-1" National Drug Code (NDC)

NDC Code	70771-1592-1
Package Description	100 CAPSULE in 1 BOTTLE (70771-1592-1)
Product NDC	70771-1592
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Atazanavir
Non-Proprietary Name	Atazanavir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20210504
Marketing Category Name	ANDA
Application Number	ANDA210575
Manufacturer	Zydus Lifesciences Limited
Substance Name	ATAZANAVIR SULFATE
Strength	200
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]