# Budesonide

NDC: 64980-638
Generic name: BUDESONIDE
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INHALANT
Routes: RESPIRATORY (INHALATION)
Marketing started: 20250314

FDA application: ANDA078202

## Active ingredients

- BUDESONIDE: .25 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64980-638"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-638
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3235e2a4-8e12-2d58-e063-6294a90a4936