NDC 69986-017

paroxetine hydrochloride 37.5 mg tablet, film coated, extended release

On the label: Sinotherapeutics Inc..

China: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Haimen Pharma Inc.Nantong, ChinaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyAug 25, 2023 · 2 inspections

Product details

Generic drug
Paroxetine: every company that makes it
Form
tablet, film coated, extended release
Strength
37.5 mg
Approval
ANDA ANDA213612
On the market since
Dec 22, 2023
Package NDCs
69986-017-01
Official label
DailyMed (National Library of Medicine), updated Oct 31, 2022

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