"47781-317-30" National Drug Code (NDC)

NDC Code	47781-317-30
Package Description	30 TABLET in 1 BOTTLE (47781-317-30)
Product NDC	47781-317
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine Extended Release
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20150714
Marketing Category Name	ANDA
Application Number	ANDA204621
Manufacturer	Alvogen Inc.
Substance Name	NEVIRAPINE
Strength	400
Strength Unit	mg/1
Pharmacy Classes	Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [EXT],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA]