United States · FDA National Drug Code directory
Flunisolide
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50742-317_139fb92c-bb10-4ee9-8572-679ac540aa27
- Product NDC
- 50742-317
- Form
- SOLUTION
- Composition / generic term
- Flunisolide
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220623
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUNISOLIDE — .25 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PUMP in 1 CARTON (50742-317-25) / 25 mL in 1 BOTTLE, PUMP · 50742-317-25
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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