# OCUPRESS
> **NDA019972** · New Drug Application · Sponsor: NOVARTIS · Approved 1990-05-23
## Drug
- **FDA Application Number:** NDA019972
- **Application type:** New Drug Application
- **Brand name:** OCUPRESS
- **Generic name:** Carteolol Hydrochloride
- **Active ingredients:** CARTEOLOL HYDROCHLORIDE
- **Dosage form:** SOLUTION/DROPS
- **Route:** OPHTHALMIC
- **Marketing status:** Discontinued
- **Sponsor:** NOVARTIS
- **First approval:** 1990-05-23
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=019972)
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