NDC 67877-729

Venlafaxine 225 mg tablet, extended release

On the label: Ascend Laboratories, LLC.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alkem Laboratories LimitedBaddi Solan, IndiaMakes it Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections

Product details

Generic drug
Venlafaxine: every company that makes it
Form
tablet, extended release, oral
Strength
225 mg
Approval
ANDA ANDA214127
On the market since
Jun 11, 2021
Package NDCs
67877-729-30 67877-729-90
Official label
DailyMed (National Library of Medicine), updated Jul 29, 2024

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