FDA NDC Directory · JSON-LD · Markdown
NDC 24338-201 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | sodium sulfate, magnesium sulfate, and potassium chloride |
|---|---|
| Labeler / Manufacturer | Azurity Pharmaceuticals, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA213135 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | MAGNESIUM SULFATE ANHYDROUS (2.7 g/1) POTASSIUM CHLORIDE (2.25 g/1) SODIUM SULFATE (17.75 g/1) |
| Marketing started | 20260401 |
| Package count | 1 |
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