NDC 0832-0817

Deflazacort 36 mg tablet

On the label: Upsher-Smith Laboratories, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bora Pharmaceuticals Inc.Maple Grove, MN, United StatesMakes it and tests it Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections

Product details

Generic drug
Deflazacort: every company that makes it
Form
tablet, oral
Strength
36 mg
Approval
ANDA ANDA216720
On the market since
Nov 5, 2024
Package NDCs
0832-0817-30
Official label
DailyMed (National Library of Medicine), updated Jul 6, 2026

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