NDC 43602-393

Venlafaxine Hydrochloride 75 mg tablet, extended release

On the label: Ascent Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Product details

Generic drug
Venlafaxine: every company that makes it
Form
tablet, extended release
Strength
75 mg
Approval
ANDA ANDA214419
On the market since
Oct 23, 2020
Package NDCs
43602-393-05 43602-393-30
Official label
DailyMed (National Library of Medicine), updated Oct 23, 2020

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