NDC 53104-0166

nevirapine 200 mg tablet

On the label: Cipla Ltd..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Cipla LimitedSalcette, IndiaMakes it Problems found, fixed voluntarilyJun 21, 2024 · 12 inspections, 2 with FDA action

Product details

Generic drug
Nevirapine: every company that makes it
Form
tablet
Strength
200 mg
Approval
ANDA ANDA077956
On the market since
May 22, 2012
Package NDCs
53104-0166-2 53104-0166-6
Official label
DailyMed (National Library of Medicine), updated Nov 27, 2018

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