NDC 50090-7173

Budesonide 0.25 mg per 2 mL inhalant

On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Nephron Pharmaceuticals Corporation's NDC 0487-9601.

United States: 1

Where the pills inside were 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

Repackaging site

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
Oct 1, 2013
Package NDCs
50090-7173-0
Official label
DailyMed (National Library of Medicine), updated May 23, 2024

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?