# BUDESONIDE
> **ANDA211922** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM · Approved 2021-04-14
## Drug
- **FDA Application Number:** ANDA211922
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** BUDESONIDE
- **Generic name:** BUDESONIDE
- **Active ingredients:** BUDESONIDE
- **Dosage form:** SUSPENSION
- **Route:** INHALATION
- **Marketing status:** Prescription
- **Sponsor:** SUN PHARM
- **Manufacturer:** Sun Pharmaceutical Industries, Inc.
- **First approval:** 2021-04-14
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211922)
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*MORVS · CC0 1.0*