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Pharmaranks rates Geodon 3.6/5 for recall safety — an independent score from its FDA recall history and its manufacturer's record. Geodon (Ziprasidone Hydrochloride) is an atypical antipsychotic used to treat Tourette Syndrome, Schizophrenia.

Ziprasidone Hydrochloride · by Viatris

72/100Limited · 1 source

Based on 1 source · Recall-safety score from FDA recall history — this product's own recalls and its manufacturer's record. Not an efficacy or quality rating. methodology →

Rated against independent regulatory sources·Last updated October 10, 2026·How we rate
Verified againstopenFDANIH DailyMedRxClass

Key facts

Active ingredient
Ziprasidone Hydrochloride
Form
Capsule, Injectable
Strength
Ziprasidone Hydrochloride EQ 20MG Base · Ziprasidone Hydrochloride EQ 40MG Base · Ziprasidone Hydrochloride EQ 60MG Base · Ziprasidone Hydrochloride EQ 80MG Base
Type
Prescription (Rx)
Brand or generic
Brand-name
Manufacturer
Viatris
What the pharmacy pays
~$9.47 for 30 — not your price
FDA application
NDA020825

Drug class

How this class works, per Atypical Antipsychotic Agents - StatPearls - NCBI Bookshelf.

May treat (source: NIH RxClass)

See how Geodon ranks — best-rated atypical antipsychotic for:

Dosage forms

Capsule and Injectable

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

What does Geodon treat?
Geodon (Ziprasidone Hydrochloride) may be used to treat tourette syndrome, schizophrenia, based on NIH RxClass drug-classification data (conditions a drug may treat — not a verbatim copy of the FDA-approved label). This is general reference, not medical advice.
How does Geodon work?
Geodon is a atypical antipsychotic. Atypical antipsychotics block dopamine D2 receptors and serotonin 5-HT2A receptors in the brain, rebalancing these signaling chemicals to reduce hallucinations, delusions, and mood symptoms in conditions like schizophrenia and bipolar disorder.
How is Geodon rated?
pharmaranks gives Geodon a composite score of 3.6 out of 5, currently based on 1 weighted source (FDA regulatory recall-safety data weighted highest). See our methodology at /how-we-rate.
How much does Geodon cost?
Nobody can tell you what you will pay — your price is set by your insurer's formulary, your deductible and the pharmacy's markup, and none of those are published. What IS published is what the pharmacy paid to acquire it: about $9.47 for 30, per the CMS NADAC survey. Treat that as the floor, not the quote — ask the pharmacist for the cash price as well as your copay, because for cheap generics the cash price often wins.
Is there a coupon or discount for Geodon?
pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Geodon. 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 Geodon?
Geodon is marketed by Viatris. You can see Viatris's full profile, rating, and other products on pharmaranks.
Is Geodon a brand-name or generic drug?
Geodon is a brand-name product with the active ingredient Ziprasidone Hydrochloride.
Is Geodon available over the counter?
No. Geodon 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 Geodon come in?
Geodon is currently marketed as capsule and injectable, per the FDA's National Drug Code Directory.
What class of drug is Geodon?
Geodon is classified as atypical antipsychotic, per the FDA's Established Pharmacologic Class.
Is Geodon FDA-registered?
Geodon is on record with the U.S. FDA under application number NDA020825. You can verify this on its official FDA label.
Has Geodon been recalled by the FDA?
Geodon has no FDA recalls recorded under its own application in the openFDA enforcement database. Its recall-safety score reflects its manufacturer's overall recall record. This is general reference, not medical advice — check the FDA recall database for the latest alerts.
Is Geodon safe?
There's no single safe-or-not verdict. pharmaranks gives Geodon a recall-safety score of 72/100, based on its FDA recall history (no recalls under its own FDA application) — not an efficacy or side-effect rating. Review its FDA-label side effects and warnings before use, and always consult a licensed professional.

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 ZIPRASIDONE HYDROCHLORIDE

The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 1,565 reports naming ZIPRASIDONE HYDROCHLORIDE — the active ingredient in Geodon, and the FDA flagged 84% 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:

  • sedation396 reports
  • dyskinesia384 reports
  • sexual dysfunction382 reports
  • dystonia376 reports
  • blood prolactin abnormal370 reports
  • anosognosia324 reports
  • blood glucose increased324 reports
  • metabolic disorder319 reports

Read these as a signal, not a rate. A report does not mean ZIPRASIDONE HYDROCHLORIDE 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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