NDC 68382-099

Paroxetine 30 mg tablet, film coated

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action
Zydus Lifesciences LimitedSolan, IndiaMakes it and tests it No problems foundMar 9, 2020 · 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
Paroxetine: every company that makes it
Form
tablet, film coated, oral
Strength
30 mg
Approval
ANDA ANDA077584
On the market since
Apr 13, 2007
Package NDCs
68382-099-01 68382-099-05 68382-099-06 68382-099-10 68382-099-16
Official label
DailyMed (National Library of Medicine), updated Jan 7, 2025

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