United States · FDA National Drug Code directory
Cyclosporine
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
- 10702-808_795f036f-ee97-42b7-bd36-fff9220ce428
- Product NDC
- 10702-808
- Form
- EMULSION
- Composition / generic term
- Cyclosporine
- Labeler
- KVK-TECH, INC.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20220210
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOSPORINE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 VIAL, SINGLE-USE in 1 TRAY (10702-808-03) / .4 mL in 1 VIAL, SINGLE-USE · 10702-808-03
- 60 VIAL, SINGLE-USE in 1 TRAY (10702-808-06) / .4 mL in 1 VIAL, SINGLE-USE · 10702-808-06
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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