flunisolide

Generic: flunisolide

Labeler: bausch & lomb incorporated
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flunisolide
Generic Name flunisolide
Labeler bausch & lomb incorporated
Dosage Form SOLUTION
Routes
NASAL
Active Ingredients

flunisolide .25 mg/mL

Manufacturer
Bausch & Lomb Incorporated

Identifiers & Regulatory

Product NDC 24208-344
Product ID 24208-344_103e2cf8-62f9-4911-995b-444bde83bcf6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074805
Listing Expiration 2026-12-31
Marketing Start 2002-02-20

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24208344
Hyphenated Format 24208-344

Supplemental Identifiers

RxCUI
1797863
UNII
QK4DYS664X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name flunisolide (source: ndc)
Generic Name flunisolide (source: ndc)
Application Number ANDA074805 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, PUMP in 1 CARTON (24208-344-25) / 25 mL in 1 BOTTLE, PUMP
source: ndc

Packages (1)

Ingredients (1)

flunisolide (.25 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "103e2cf8-62f9-4911-995b-444bde83bcf6", "openfda": {"unii": ["QK4DYS664X"], "rxcui": ["1797863"], "spl_set_id": ["7c72c954-3758-40c3-9977-d03b25d71e0a"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (24208-344-25)  / 25 mL in 1 BOTTLE, PUMP", "package_ndc": "24208-344-25", "marketing_start_date": "20020220"}], "brand_name": "Flunisolide", "product_id": "24208-344_103e2cf8-62f9-4911-995b-444bde83bcf6", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "24208-344", "generic_name": "Flunisolide", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flunisolide", "active_ingredients": [{"name": "FLUNISOLIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA074805", "marketing_category": "ANDA", "marketing_start_date": "20020220", "listing_expiration_date": "20261231"}