# SUPREP BOWEL PREP KIT
> **NDA022372** · New Drug Application · Sponsor: AZURITY · Approved 2010-08-05
## Drug
- **FDA Application Number:** NDA022372
- **Application type:** New Drug Application
- **Brand name:** SUPREP BOWEL PREP KIT
- **Generic name:** SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE
- **Active ingredients:** MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE
- **Dosage form:** SOLUTION
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** AZURITY
- **Manufacturer:** Azurity Pharmaceuticals, Inc.
- **First approval:** 2010-08-05
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=022372)
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