NDC 64980-638

Budesonide 0.25 mg per 2 mL inhalant

On the label: Rising Pharma Holdings, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Nephron SC, LLCWest Columbia, SC, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyAug 22, 2025 · 26 inspections, 10 with FDA action

Product details

Generic drug
Budesonide: every company that makes it
Form
inhalant, respiratory (inhalation)
Strength
0.25 mg per 2 mL
Approval
ANDA ANDA078202
On the market since
Mar 14, 2025
Package NDCs
64980-638-03
Official label
DailyMed (National Library of Medicine), updated Jul 16, 2026

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