NDC 69584-672

paroxetine hydrochloride 20 mg tablet, film coated

On the label: Oxford Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Product details

Generic drug
Paroxetine: every company that makes it
Form
tablet, film coated, oral
Strength
20 mg
Approval
ANDA ANDA076968
On the market since
Nov 14, 2022
Package NDCs
69584-672-03 69584-672-09 69584-672-10 69584-672-50 69584-672-90
Official label
DailyMed (National Library of Medicine), updated Aug 9, 2024

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