"70771-1745-5" National Drug Code (NDC)

NDC Code	70771-1745-5
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (70771-1745-5)
Product NDC	70771-1745
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Darunavir
Non-Proprietary Name	Darunavir
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20240501
Marketing Category Name	ANDA
Application Number	ANDA214085
Manufacturer	Zydus Lifesciences Limited
Substance Name	DARUNAVIR
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], HIV Protease Inhibitors [MoA], Protease Inhibitor [EPC]