# VYZULTA
> **NDA207795** · New Drug Application · Sponsor: BAUSCH AND LOMB · Approved 2017-11-02
## Drug
- **FDA Application Number:** NDA207795
- **Application type:** New Drug Application
- **Brand name:** VYZULTA
- **Generic name:** LATANOPROSTENE BUNOD
- **Active ingredients:** LATANOPROSTENE BUNOD
- **Dosage form:** SOLUTION/DROPS
- **Route:** OPHTHALMIC
- **Marketing status:** Prescription
- **Sponsor:** BAUSCH AND LOMB
- **Manufacturer:** Bausch & Lomb Incorporated
- **First approval:** 2017-11-02
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=207795)
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