NDC 50090-5145

venlafaxine hydrochloride 75 mg capsule, extended release

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-035.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Venlafaxine: every company that makes it
Form
capsule, extended release
Strength
75 mg
Approval
ANDA ANDA090174
On the market since
Jun 1, 2011
Package NDCs
50090-5145-0
Official label
DailyMed (National Library of Medicine), updated Mar 2, 2021

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