# UNIRETIC
> **NDA020729** · New Drug Application · Sponsor: UCB INC · Approved 1997-06-27
## Drug
- **FDA Application Number:** NDA020729
- **Application type:** New Drug Application
- **Brand name:** UNIRETIC
- **Generic name:** Hydrochlorothiazide
- **Active ingredients:** HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** UCB INC
- **First approval:** 1997-06-27
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=020729)
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