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
- 0172-7313_94a2cdae-e60e-47c4-8bca-8baac9f21b33
- Product NDC
- 0172-7313
- Form
- SOLUTION
- Composition / generic term
- Cyclosporine
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050329
- Source listing expiry
- 20261231
Source-listed ingredients
- CYCLOSPORINE — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 PACKAGE (0172-7313-20) / 50 mL in 1 BOTTLE · 0172-7313-20
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 →