NDC 0245-0813

Kymbee 22.75 mg per 1 mL suspension

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 Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections

Product details

Generic drug
Deflazacort: every company that makes it
Form
suspension, oral
Strength
22.75 mg per 1 mL
Approval
ANDA ANDA216992
On the market since
Jun 5, 2026
Package NDCs
0245-0813-13
Official label
DailyMed (National Library of Medicine), updated Jun 18, 2026

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