← FDA Drug Approvals (Drugs@FDA)
SUPREP BOWEL PREP KIT
NDA · New Drug Application · Sponsor: AZURITY · Approved 2010-08-05
Drug application
- FDA Application #
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
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown