# IOSAT

NDC: 51803-002
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: 20130501

FDA application: NDA018664

## Active ingredients

- POTASSIUM IODIDE: 65 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51803-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51803-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bab815ee-47ef-4c87-a60d-e0d7863ad871