"65862-057-11" National Drug Code (NDC)

NDC Code	65862-057-11
Package Description	100 mL in 1 BOTTLE (65862-057-11)
Product NDC	65862-057
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20120522
Marketing Category Name	ANDA
Application Number	ANDA077702
Manufacturer	Aurobindo Pharma Limited
Substance Name	NEVIRAPINE HEMIHYDRATE
Strength	50
Strength Unit	mg/5mL
Pharmacy Classes	Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]