"69097-233-46" National Drug Code (NDC)

NDC Code	69097-233-46
Package Description	240 mL in 1 BOTTLE (69097-233-46)
Product NDC	69097-233
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20170803
Marketing Category Name	ANDA
Application Number	ANDA207684
Manufacturer	Cipla USA Inc.
Substance Name	NEVIRAPINE HEMIHYDRATE
Strength	50
Strength Unit	mg/5mL
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]