NDC 80425-0371

Desonide 0.5 mg per 1 g cream

On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-086.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it No problems foundFeb 14, 2025 · 4 inspections

Repackaging site

Product details

Generic drug
Desonide: every company that makes it
Form
cream, topical
Strength
0.5 mg per 1 g
Approval
ANDA ANDA210198
On the market since
Dec 7, 2023
Package NDCs
80425-0371-1
Official label
DailyMed (National Library of Medicine), updated Dec 31, 2024

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