sodium iodide i 123
Sodium Iodide I 123 (Sodium Iodide I-123) is a medication supplied as a capsule, gelatin coated.
Sodium Iodide I-123 · by Ge Healthcare
Key facts
- Active ingredient
- Sodium Iodide I-123
- Form
- Capsule
- Strength
- Sodium Iodide I-123 100uCi · Sodium Iodide I-123 200uCi · Sodium Iodide I-123 2mCi/ML **Federal Register Determination That Product was not Discontinued or Withdrawn for Safety or Effectiveness reasons**
- Type
- Prescription (Rx)
- Brand or generic
- Brand-name
- Manufacturer
- Ge Healthcare
- FDA application
- NDA017630
- Availability
- Discontinued (per FDA)
Dosage forms
Capsule
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
Ask for the generic
Same active ingredient, far cheaper. Is there a generic? →
Request a 90-day supply
Bulk fills usually lower the per-dose price vs monthly refills.
Use copay cards
Manufacturer copay cards & patient-assistance programs — especially for brand drugs.
Compare alternatives
A same-class option may cost less. See alternatives →
Frequently asked questions
- Is there a coupon or discount for Sodium Iodide I 123?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Sodium Iodide I 123. To pay less, ask your prescriber or pharmacist whether a generic equivalent exists, check the manufacturer's copay/savings card and patient-assistance program, and compare a pharmacy discount card against your insurance copay. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
- Who makes Sodium Iodide I 123?
- Sodium Iodide I 123 is marketed by Ge Healthcare. You can see Ge Healthcare's full profile, rating, and other products on pharmaranks.
- Is Sodium Iodide I 123 a brand-name or generic drug?
- Sodium Iodide I 123 is a brand-name product with the active ingredient Sodium Iodide I-123.
- Is Sodium Iodide I 123 available over the counter?
- No. Sodium Iodide I 123 is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
- What forms does Sodium Iodide I 123 come in?
- Sodium Iodide I 123 is currently marketed as capsule, per the FDA's National Drug Code Directory.
- Is Sodium Iodide I 123 FDA-registered?
- Sodium Iodide I 123 is on record with the U.S. FDA under application number NDA017630. You can verify this on its official FDA label.
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about SODIUM IODIDE I-123
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 58 reports naming SODIUM IODIDE I-123 — the active ingredient in Sodium Iodide I 123, and the FDA flagged 28% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- urticaria7 reports
- rash6 reports
- headache5 reports
- pruritus5 reports
- dyspnoea4 reports
- nausea4 reports
- anaphylactic shock3 reports
- chest pain3 reports
Read these as a signal, not a rate. A report does not mean SODIUM IODIDE I-123 caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.
Source: openFDA drug/event (FAERS), retrieved September 26, 2026.
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