# OXYBUTYNIN CHLORIDE
> **ANDA206121** · Abbreviated New Drug Application (Generic) · Sponsor: UNIQUE · Approved 2016-05-27
## Drug
- **FDA Application Number:** ANDA206121
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** OXYBUTYNIN CHLORIDE
- **Generic name:** OXYBUTYNIN CHLORIDE
- **Active ingredients:** OXYBUTYNIN CHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** UNIQUE
- **Manufacturer:** Rising Pharma Holdings, Inc.
- **First approval:** 2016-05-27
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=206121)
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