# Budesonide Inhalation

NDC: 0115-1687
Generic name: Budesonide
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: RESPIRATORY (INHALATION)
Marketing started: 20160804

FDA application: ANDA078404

## Active ingredients

- BUDESONIDE: .25 mg/2mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-1687"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-1687
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e8ef9489-83a2-4817-b21c-ea3fecd8c8dd