NDC 0615-8359

Paroxetine 10 mg tablet, film coated

On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Aurolife Pharma LLC's NDC 13107-154.

India: 1United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action
Aurolife Pharma LLCDayton, NJ, United StatesMakes it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Paroxetine: every company that makes it
Form
tablet, film coated, oral
Strength
10 mg
Approval
ANDA ANDA078406
On the market since
Dec 3, 2009
Package NDCs
0615-8359-39
Official label
DailyMed (National Library of Medicine), updated Sep 2, 2022

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