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
- 71656-012_458a84bc-12a1-5159-e063-6394a90ac45c
- Product NDC
- 71656-012
- Form
- EMULSION
- Composition / generic term
- CYCLOSPORINE
- Labeler
- Saptalis Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251212
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOSPORINE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 6 POUCH in 1 CARTON (71656-012-30) / 5 VIAL, SINGLE-DOSE in 1 POUCH / .4 mL in 1 VIAL, SINGLE-DOSE · 71656-012-30
- 12 POUCH in 1 CARTON (71656-012-60) / 5 VIAL, SINGLE-DOSE in 1 POUCH / .4 mL in 1 VIAL, SINGLE-DOSE · 71656-012-60
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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