FDA NDC Directory · JSON-LD · Markdown
NDC 24338-175 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE
| Generic name | sodium sulfate, potassium sulfate, magnesium sulfate |
|---|---|
| Labeler / Manufacturer | Azurity Pharmaceuticals, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA022372 |
| Dosage form / route | SOLUTION, CONCENTRATE · ORAL |
| Active ingredients | MAGNESIUM SULFATE, UNSPECIFIED FORM (1.6 g/mL) POTASSIUM SULFATE (3.13 g/mL) SODIUM SULFATE (17.5 g/mL) |
| Marketing started | 20260401 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).