# Budesonide

NDC: 60687-889
Generic name: Budesonide
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20260503

FDA application: ANDA211922

## Active ingredients

- BUDESONIDE: .25 mg/2mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-889"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-889
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c7df2a10-4166-423e-bb60-5f3a8234f26c