NDC 68071-2704

Desvenlafaxine 50 mg tablet, extended release

On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Breckenridge Pharmaceutical, Inc.'s NDC 51991-311.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Alembic Pharmaceuticals LimitedPanchmahal, IndiaMakes it No problems foundJul 26, 2024 · 8 inspections

Repackaging site

Product details

Generic drug
Desvenlafaxine: every company that makes it
Form
tablet, extended release
Strength
50 mg
Approval
ANDA ANDA204003
On the market since
Mar 1, 2017
Package NDCs
68071-2704-3
Official label
DailyMed (National Library of Medicine), updated May 19, 2022

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