NDC 0832-0285

Bexarotene 75 mg capsule

On the label: Upsher-Smith Laboratories, Inc..

New Zealand: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Douglas Manufacturing LimitedLincoln Auckland, New ZealandMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 30, 2025 · 6 inspections

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Bexarotene: every company that makes it
Form
capsule, oral
Strength
75 mg
Approval
ANDA ANDA209886
On the market since
Jul 25, 2018
Package NDCs
0832-0285-00
Official label
DailyMed (National Library of Medicine), updated Mar 31, 2023

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