# Cyclosporine

NDC: 0480-4076
Generic name: Cyclosporine
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: EMULSION
Routes: OPHTHALMIC
Marketing started: 20251028

FDA application: ANDA203880

## Active ingredients

- CYCLOSPORINE: .5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0480-4076"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-4076
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cc64c1e3-19f5-4bf6-a08d-a9725004c97f