United States · FDA National Drug Code directory

Cyclosporine Modified

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
0093-9019_d5d977b4-fc80-4e46-ab55-280fd6d4ea12
Product NDC
0093-9019
Form
CAPSULE, LIQUID FILLED
Composition / generic term
Cyclosporine
Labeler
Teva Pharmaceuticals USA, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20210608
Source listing expiry
20261231

Source-listed ingredients

  • CYCLOSPORINE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 BLISTER PACK in 1 CARTON (0093-9019-65) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0093-9019-19) · 0093-9019-65

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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