"65862-933-05" National Drug Code (NDC)

NDC Code	65862-933-05
Package Description	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65862-933-05)
Product NDC	65862-933
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20170228
Marketing Category Name	ANDA
Application Number	ANDA207698
Manufacturer	Aurobindo Pharma Limited
Substance Name	NEVIRAPINE
Strength	400
Strength Unit	mg/1
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]