← FDA Drug Approvals (Drugs@FDA)
NULYTELY
NDA · New Drug Application · Sponsor: AZURITY · Approved 1991-04-22
Drug application
- FDA Application #
NDA019797- Application type
- New Drug Application
- Brand name
- NULYTELY
- Generic name
- POLYETHYLENE GLYCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE
- Active ingredients
- POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
- Dosage form
- FOR SOLUTION
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- AZURITY
- Manufacturer
- Wilshire Pharmaceuticals, Inc.
- First approval
- 1991-04-22
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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