"53808-0680-1" National Drug Code (NDC)

NDC Code	53808-0680-1
Package Description	30 TABLET in 1 BLISTER PACK (53808-0680-1)
Product NDC	53808-0680
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130101
Marketing Category Name	ANDA
Application Number	ANDA202523
Manufacturer	State of Florida DOH Central Pharmacy
Substance Name	NEVIRAPINE
Strength	200
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]