# Budesonide

NDC: 50090-7173
Generic name: BUDESONIDE
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INHALANT
Routes: RESPIRATORY (INHALATION)
Marketing started: 20131001

FDA application: ANDA078202

## Active ingredients

- BUDESONIDE: .25 mg/2mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-7173"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7173
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=521a79d0-4d93-45f7-8feb-8d2b502dd216