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Nevirapine

NDC 65862-057 · Aurobindo Pharma Limited

Generic nameNevirapine
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)NEVIRAPINE HEMIHYDRATE
Strength50 mg/5mL
Pharmacologic classCytochrome P450 2B6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]
Marketing categoryANDA

Packages

65862-057-11 — 100 mL in 1 BOTTLE (65862-057-11)

65862-057-24 — 240 mL in 1 BOTTLE (65862-057-24)

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.