FDA NDC Directory · JSON-LD · Markdown
NDC 50633-920 · HUMAN OTC DRUG · TABLET
| Generic name | Potassium iodide |
|---|---|
| Labeler / Manufacturer | BTG International Inc |
| Marketing category | Abbreviated NDA (generic) · App ANDA076350 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | POTASSIUM IODIDE (130 mg/1) |
| Marketing started | 20251126 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).