NDC 24208-344

Flunisolide

Flunisolide

Flunisolide is a Nasal Solution in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Flunisolide.

Product ID24208-344_cd97aa97-0d80-4f70-8c74-461caa23e12b
NDC24208-344
Product TypeHuman Prescription Drug
Proprietary NameFlunisolide
Generic NameFlunisolide
Dosage FormSolution
Route of AdministrationNASAL
Marketing Start Date2002-02-20
Marketing CategoryANDA / ANDA
Application NumberANDA074805
Labeler NameBausch & Lomb Incorporated
Substance NameFLUNISOLIDE
Active Ingredient Strength0 mg/mL
Pharm ClassesCorticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 24208-344-25

1 BOTTLE, PUMP in 1 CARTON (24208-344-25) > 25 mL in 1 BOTTLE, PUMP
Marketing Start Date2002-02-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 24208-344-25 [24208034425]

Flunisolide SOLUTION
Marketing CategoryANDA
Application NumberANDA074805
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2002-02-20

Drug Details

Active Ingredients

IngredientStrength
FLUNISOLIDE.25 mg/mL

OpenFDA Data

SPL SET ID:7c72c954-3758-40c3-9977-d03b25d71e0a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1797863
  • Pharmacological Class

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

    Medicade Reported Pricing

    24208034425 FLUNISOLIDE 0.025% SPRAY

    Pricing Unit: ML | Drug Type:

    NDC Crossover Matching brand name "Flunisolide" or generic name "Flunisolide"

    NDCBrand NameGeneric Name
    24208-344FlunisolideFlunisolide
    50742-317FlunisolideFlunisolide
    64980-510FlunisolideFlunisolide
    70518-0671FlunisolideFlunisolide
    0037-7590Aerospanflunisolide

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.