"69097-403-02" National Drug Code (NDC)

NDC Code	69097-403-02
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-403-02)
Product NDC	69097-403
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20151015
End Marketing Date	20191231
Marketing Category Name	ANDA
Application Number	ANDA206448
Manufacturer	Cipla USA 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]