# IOSAT

NDC: 51803-001
Generic name: Potassium Iodide
Labeler / Manufacturer: Anbex Inc.
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19821014

FDA application: NDA018664

## Active ingredients

- POTASSIUM IODIDE: 130 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51803-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51803-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ea98aef8-93b6-4fac-be35-eb17a1a04a92