50742-317 : Flunisolide .25 mg/ml Nasal Solution


NDC: 50742-317
Labeler: Ingenus Pharmaceuticals, LLC
Product Type: Human Prescription Drug
Drug Name:  Flunisolide
Dosage Form: Nasal Solution
Application #: ANDA207802
Rev. Date: 


NDC Package Codes:

  • 50742-317-25: 1 BOTTLE, PUMP IN 1 CARTON (50742‑317‑25) > 25 ML IN 1 BOTTLE, PUMP

Active Ingredients:

  • Flunisolide

Dosage Strength:

  • .25 mg/mL

Pharmaceutical Classes:

  • Corticosteroid Hormone Receptor Agonists [MoA]
  • Corticosteroid [EPC]

Related Products:

Based on records with the same trade name.
  • 24208-344 Flunisolide .25 mg/ml Nasal Solution by Bausch & Lomb Incorporated
  • 54868-4799 Flunisolide .25 mg/ml Nasal Solution by Physicians Total Care, Inc.
  • 60505-0824 Flunisolide 29 ug/1 Nasal Spray, Metered by Apotex Corp.
  • 61786-597 Flunisolide .25 mg/ml Nasal Solution by Remedyrepack Inc.
  • 64980-506 Flunisolide .25 mg/ml Nasal Spray, Metered by Rising Pharmaceuticals, Inc
  • 64980-510 Flunisolide .25 mg/ml Nasal Spray, Metered by Rising Pharmaceuticals, Inc
  • 70518-0671 Flunisolide .25 mg/ml Nasal Solution by Remedyrepack Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.