NDC 68788-8503

budesonide inhalation 0.5 mg per 2 mL suspension

On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-984.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
The Ritedose CorporationColumbia, SC, United StatesMakes it and packages it Problems found, fixed voluntarilyFeb 28, 2025 · 12 inspections

Repackaging site

Product details

Generic drug
Budesonide: every company that makes it
Form
suspension, respiratory (inhalation)
Strength
0.5 mg per 2 mL
Approval
ANDA ANDA210897
On the market since
Aug 9, 2023
Package NDCs
68788-8503-3
Official label
DailyMed (National Library of Medicine), updated Mar 20, 2026

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