NDC 62135-823

Budesonide 0.5 mg per 2 mL suspension

On the label: Chartwell RX, LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Nephron SC, LLCWest Columbia, SC, United StatesMakes it Problems found, fixed voluntarilyAug 22, 2025 · 26 inspections, 10 with FDA action
Chartwell Pharmaceuticals Congers, LLC.Congers, NY, United StatesPackages it Serious problems, FDA actionNov 18, 2025 · 8 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 ANDA078202
On the market since
Oct 1, 2013
Package NDCs
62135-823-84
Official label
DailyMed (National Library of Medicine), updated Feb 2, 2024

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