FDA NDC Directory · JSON-LD · Markdown

IOSAT

NDC 51803-002 · HUMAN OTC DRUG · TABLET

Generic namePotassium Iodide
Labeler / ManufacturerAnbex Inc.
Marketing categoryNew Drug Application (innovator) · App NDA018664
Dosage form / routeTABLET · ORAL
Active ingredientsPOTASSIUM IODIDE (65 mg/1)
Marketing started20130501
Package count2

External sources

Source: openFDA. Public-domain (CC0).