Medicine
Geodon 80 mg capsule
Geodon 80 mg capsule is a prescription medicine containing Ziprasidone for oral use, marketed by Viatris Specialty, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.
Availability
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
They are supplied in the following strengths and package configurations…
Key facts
- Active ingredient (INN)
- Ziprasidone
- Brand
- Geodon
- Strength
- 80 mg
- Dosage form
- Capsule
- Route
- Oral
- Packs
- 60 capsules
- Marketing authorisation holder
- Viatris Specialty
- Manufacturers
- Viatris SpecialtyRoerig
- Origin register
- US FDA, United States
- Storage
- They are supplied in the following strengths and package configurations: GEODON Capsules Package Configuration Capsule Strength (mg) NDC (National Drug Code) Imprint Bottles of 60 20 0049-0052-60 or 0049-0352-60 ZDX 20 Bottles of 60 40 0049-0054-60 or 0049-0354-60 ZDX 40 Bottles of 60 60 0049-0056-60 or 0049-0356-60 ZDX 60 Bottles of 60 80 0049-0058-60 or 0049-0358-60 ZDX 80 or GEODON Capsules…
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- N05AE04 Ziprasidone
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 8 November 2021
- Identifiers
- RxCUI 284548, 284549, 284550 +7DailyMed set ID 8326928a-2cb6-4f7f-9712-03a425a14c37, a2b4cc65-6a6d-49c4-adfc-a4458562a167NDC 0049-0358, 58151-134Application NDA020825
Record updated 12 November 2026
Documents available
Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.
No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.
Packs
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 60 capsule in 1 bottle | 58151-134-91 | Viatris Specialty | 15 April 2026 |
| 60 capsule in 1 bottle | 0049-0358-60 | Roerig | 8 November 2021 |
Status by register
Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| US FDA | First approved 5 February 2001 | Drugs@FDA |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US FDA (NDC directory, openFDA)Checked 12 November 2026 |
Import route
Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.
Import guides are available for 25 countries. Pick one to see its route summary.
BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides
Alternatives
Other makers and brands of Ziprasidone 80 mg capsule.
Other strengths and forms of Ziprasidone
Clinical summary
Ziprasidone is an atypical antipsychotic indicated for the treatment of schizophrenia, among other approved uses. It is available as capsules and powder for injection for oral and intramuscular use. MedsAcross supplies Ziprasidone for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.
Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review
Read about ZiprasidoneFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Geodon prescribing information (Viatris Specialty) · U.S. National Library of Medicine, DailyMed
Need Geodon 80 mg capsule for your hospital or patient?
Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.