NDC 59651-585

Budesonide 0.5 mg per 2 mL suspension

On the label: Aurobindo Pharma Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Eugia Pharma Specialities LimitedSangareddy, IndiaMakes it, tests it and packages it Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action

Product details

Generic drug
Budesonide: every company that makes it
Form
suspension, respiratory (inhalation)
Strength
0.5 mg per 2 mL
Approval
ANDA ANDA216667
On the market since
Nov 29, 2023
Package NDCs
59651-585-05 59651-585-30
Official label
DailyMed (National Library of Medicine), updated Dec 2, 2023

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