NDC 68071-2703

Venlafaxine Hydrochloride 75 mg capsule, extended release

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-003.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Annora Pharma Private LimitedSangareddy, IndiaMakes it Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections

Repackaging site

Product details

Generic drug
Venlafaxine: every company that makes it
Form
capsule, extended release
Strength
75 mg
Approval
ANDA ANDA212277
On the market since
Jul 8, 2019
Package NDCs
68071-2703-3
Official label
DailyMed (National Library of Medicine), updated May 20, 2022

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