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
- 60505-6202_58c5fb86-01c3-497b-86f7-a65055732970
- Product NDC
- 60505-6202
- Form
- EMULSION
- Composition / generic term
- Cyclosporine
- Labeler
- Apotex Corp
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20220207
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOSPORINE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 VIAL in 1 TRAY (60505-6202-1) / .4 mL in 1 VIAL · 60505-6202-1
- 60 VIAL in 1 TRAY (60505-6202-2) / .4 mL in 1 VIAL · 60505-6202-2
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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