Medicine
Ultravist 185000 mg/500 mL injection
Ultravist 185000 mg/500 mL injection is a prescription medicine containing Iopromide for intra-arterial, intravenous use, marketed by Bayer HealthCare Pharmaceuticals, 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
Store at 25°C (77°F), excursions permitted to 15°C to 30°C (59°F to 86°F)…
Key facts
- Active ingredient (INN)
- Iopromide
- Brand
- Ultravist
- Strength
- 185000 mg/500 mL
- Dosage form
- Injection
- Route
- Intra-arterial, intravenous
- Packs
- 8 bottles of 500 mL
- Marketing authorisation holder
- Bayer HealthCare Pharmaceuticals
- Manufacturer
- Bayer HealthCare Pharmaceuticals
- Origin register
- US FDA, United States
- Storage
- Store at 25°C (77°F), excursions permitted to 15°C to 30°C (59°F to 86°F). Protect from light.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- ATC code
- V08AB05 Iopromide
- HS code (indicative)
- 3004.90Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 30 December 2009
- Identifiers
- DailyMed set ID df917c3a-59a2-4ed1-8470-8a5394c73325NDC 50419-346Application NDA020220
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 |
|---|---|---|---|
| 8 bottle in 1 package / 500 mL in 1 bottle | 50419-346-58 | Bayer HealthCare Pharmaceuticals | 30 December 2009 |
| 8 bottle in 1 package / 500 mL in 1 bottle | 50419-346-65 | Bayer HealthCare Pharmaceuticals | 4 May 2018 |
| 8 bottle in 1 package / 500 mL in 1 bottle | 50419-346-97 | Bayer HealthCare Pharmaceuticals | 30 December 2009 |
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 10 May 1995 | 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
Other strengths and forms of Iopromide
Clinical summary
Iopromide is a radiographic contrast agent indicated for uLTRAVIST is a radiographic contrast agent indicated for, among other approved uses. It is available as injection for intra-arterial and intravenous use. MedsAcross supplies Iopromide 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 IopromideFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- Ultravist prescribing information (Bayer HealthCare Pharmaceuticals) · U.S. National Library of Medicine, DailyMed
Need Ultravist 185000 mg/500 mL injection 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.