# CEQUA

NDC: 47335-507
Generic name: cyclosporine
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC, TOPICAL
Marketing started: 20180815

FDA application: NDA210913

## Active ingredients

- CYCLOSPORINE: .0009 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-507"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-507
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48c3d8a3-4289-4b52-9189-58b48596095c