# Difluprednate

NDC: 0832-6054
Generic name: Difluprednate
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: EMULSION
Routes: OPHTHALMIC
Marketing started: 20250221

FDA application: ANDA218191

## Active ingredients

- DIFLUPREDNATE: .5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0832-6054"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-6054
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce8c1d56-771e-45da-8a19-5f881f993738