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
- 24979-126_8bf257be-d4c8-4694-b62b-f05124d378d0
- Product NDC
- 24979-126
- Form
- EMULSION
- Composition / generic term
- cyclosporine
- Labeler
- Upsher-Smith Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260327
- Source listing expiry
- 20271231
Source-listed ingredients
- CYCLOSPORINE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 60 VIAL, SINGLE-USE in 1 CARTON (24979-126-18) / .4 mL in 1 VIAL, SINGLE-USE · 24979-126-18
- 30 VIAL, SINGLE-USE in 1 CARTON (24979-126-19) / .4 mL in 1 VIAL, SINGLE-USE · 24979-126-19
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 →