Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Astrea Monts | Monts, France | Makes it and packages it | Serious problems, FDA actionOct 18, 2022 · 4 inspections, 1 with FDA action |
| Jubilant HollisterStier General Partnership | Kirkland, Canada | Makes it and packages it | Serious problems, FDA actionNov 3, 2025 · 10 inspections, 4 with FDA action |
| Simafex | Marans, France | Makes the active ingredient | Problems found, fixed voluntarilyJan 31, 2025 · 5 inspections |
| Ifts | Foulayronnes, France | Tests it | Problems found, fixed voluntarilyJul 29, 2021 · 2 inspections |
Product details
- Generic drug
- Iodine: every company that makes it
- Form
- injection, intra-arterial; intralymphatic; intrauterine
- Strength
- 480 mg per 1 mL
- Approval
- NDA NDA009190
- On the market since
- Mar 21, 2014
- Package NDCs
67684-1901-167684-1901-2- Official label
- DailyMed (National Library of Medicine), updated Dec 16, 2025
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