United States · FDA National Drug Code directory
Verkazia
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
- 65086-001_2becea0d-7cbe-6b23-e063-6294a90a5a67
- Product NDC
- 65086-001
- Form
- EMULSION
- Composition / generic term
- cyclosporine
- Labeler
- Santen Incorporated
- Marketing category
- NDA
- Marketing start / end (source format)
- 20220201
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOSPORINE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 CARTON (65086-001-05) / 5 VIAL, SINGLE-DOSE in 1 POUCH / .3 mL in 1 VIAL, SINGLE-DOSE · 65086-001-05
- 24 POUCH in 1 CARTON (65086-001-12) / 5 VIAL, SINGLE-DOSE in 1 POUCH / .3 mL in 1 VIAL, SINGLE-DOSE · 65086-001-12
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 →