# Cyclosporine

NDC: 0378-8760
Generic name: cyclosporine
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: EMULSION
Routes: OPHTHALMIC
Marketing started: 20220203

FDA application: ANDA205894

## 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:"0378-8760"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-8760
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da3fa070-b512-4568-871a-dc8d5a949d13