# Flunisolide

NDC: 50742-317
Generic name: Flunisolide
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: NASAL
Marketing started: 20220623

FDA application: ANDA207802

## Active ingredients

- FLUNISOLIDE: .25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-317"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-317
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f39cae46-c68f-47ef-82f3-4fd3dd46c74c