# OXYBUTYNIN CHLORIDE
> **ANDA202332** · Abbreviated New Drug Application (Generic) · Sponsor: ZYDUS PHARMS · Approved 2017-06-26
## Drug
- **FDA Application Number:** ANDA202332
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** OXYBUTYNIN CHLORIDE
- **Generic name:** OXYBUTYNIN
- **Active ingredients:** OXYBUTYNIN CHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** ZYDUS PHARMS
- **Manufacturer:** Zydus Pharmaceuticals USA Inc.
- **First approval:** 2017-06-26
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=202332)
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