United States · FDA National Drug Code directory

Optiray 350

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
0019-1333_471b778f-d9cc-ff10-e063-6394a90a27c9
Product NDC
0019-1333
Form
INJECTION
Composition / generic term
Ioversol
Labeler
Liebel-Flarsheim Company LLC
Marketing category
NDA
Marketing start / end (source format)
20201118
Source listing expiry
20261231

Source-listed ingredients

  • IOVERSOL — 741 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 BOTTLE, GLASS in 1 CARTON (0019-1333-65) / 500 mL in 1 BOTTLE, GLASS · 0019-1333-65

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 →