United States · FDA National Drug Code directory
Iodixanol
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 65219-383_1980ecbd-58c9-4176-af7f-af955bb0ad2e
- Product NDC
- 65219-383
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Iodixanol
- Labeler
- FRESENIUS KABI USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220621
- Source listing expiry
- 20261231
Source-listed ingredients
- IODIXANOL — 320 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BOTTLE, PLASTIC in 1 BOX (65219-383-05) / 50 mL in 1 BOTTLE, PLASTIC (65219-383-02) · 65219-383-05
- 10 BOTTLE, PLASTIC in 1 BOX (65219-383-10) / 100 mL in 1 BOTTLE, PLASTIC (65219-383-04) · 65219-383-10
- 10 BOTTLE, PLASTIC in 1 BOX (65219-383-50) / 150 mL in 1 BOTTLE, PLASTIC (65219-383-06) · 65219-383-50
- 10 BOTTLE, PLASTIC in 1 BOX (65219-383-70) / 200 mL in 1 BOTTLE, PLASTIC (65219-383-08) · 65219-383-70
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →