# OXYBUTYNIN CHLORIDE
> **ANDA213550** · Abbreviated New Drug Application (Generic) · Sponsor: REGCON HOLDINGS · Approved 2022-07-14
## Drug
- **FDA Application Number:** ANDA213550
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** OXYBUTYNIN CHLORIDE
- **Generic name:** Oxybutynin Chloride
- **Active ingredients:** OXYBUTYNIN CHLORIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** REGCON HOLDINGS
- **First approval:** 2022-07-14
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=213550)
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*MORVS · CC0 1.0*