"13925-500-60" National Drug Code (NDC)

NDC Code	13925-500-60
Package Description	60 TABLET in 1 BOTTLE (13925-500-60)
Product NDC	13925-500
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120521
End Marketing Date	20140430
Marketing Category Name	ANDA
Application Number	ANDA203176
Manufacturer	Seton Pharmaceuticals
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 [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]