United States · FDA National Drug Code directory
FLUORESCITE
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
- 0065-0092_b315434c-5397-4a9d-859e-ebd2a68ed2c3
- Product NDC
- 0065-0092
- Form
- INJECTION, SOLUTION
- Composition / generic term
- fluorescein sodium
- Labeler
- Alcon, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 19720915
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUORESCEIN SODIUM — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 VIAL in 1 CARTON (0065-0092-65) / 5 mL in 1 VIAL · 0065-0092-65
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 →