NEVIRAPINE
NDC 42571-131 · Micro Labs Limited
Generic nameNEVIRAPINE
Dosage formTABLET
RouteORAL
Active ingredient(s)NEVIRAPINE
Strength200 mg/1
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
42571-131-29 — 6 BLISTER PACK in 1 CARTON (42571-131-29) / 10 TABLET in 1 BLISTER PACK
42571-131-60 — 60 TABLET in 1 BOTTLE (42571-131-60)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0378-4050 — nevirapine, 0378-4890 — nevirapine, 31722-505 — Nevirapine, 33342-004 — Nevirapine, 33342-238 — NEVIRAPINE, 65162-209 — Nevirapine, 65862-027 — Nevirapine