NDC 43386-089

voriconazole 200 mg tablet, film coated

On the label: Lupin Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novel Laboratories, Inc.Somerset, NJ, United StatesMakes it and tests it Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Voriconazole: every company that makes it
Form
tablet, film coated, oral
Strength
200 mg
Approval
ANDA ANDA207371
On the market since
May 24, 2016
Package NDCs
43386-089-03 43386-089-05 43386-089-30 43386-089-31
Official label
DailyMed (National Library of Medicine), updated Jan 31, 2024

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