United States · FDA National Drug Code directory
Fluorescein
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
- 14789-122_b66b331e-c90a-48e0-9d9d-961c1cb5c9e2
- Product NDC
- 14789-122
- Form
- INJECTION
- Composition / generic term
- Fluorescein
- Labeler
- Nexus Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231024
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUORESCEIN — 500 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (14789-122-05) / 5 mL in 1 VIAL (14789-122-07) · 14789-122-05
Source and coverage
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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.
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