Valsts: Amerikas Savienotās Valstis
Valoda: angļu
Klimata pārmaiņas: NLM (National Library of Medicine)
FLUNISOLIDE (UNII: QK4DYS664X) (FLUNISOLIDE ANHYDROUS - UNII:78M02AA8KF)
Bausch & Lomb Incorporated
FLUNISOLIDE
FLUNISOLIDE 0.25 mg in 1 mL
NASAL
PRESCRIPTION DRUG
Flunisolide Nasal Solution is indicated for the treatment of the nasal symptoms of seasonal or perennial rhinitis. Flunisolide Nasal Solution should not be used in the presence of untreated localized infection involving nasal mucosa. Hypersensitivity to any of the ingredients.
Flunisolide Nasal Solution, USP 0.025% is supplied in a nasal pump dispenser with dust cover and with patient instructions in the following size: Each 25 mL Flunisolide Nasal Solution spray bottle contains 6.25 mg (0.25 mg/mL), 200 metered sprays of flunisolide. Storage: Store between 15° to 25°C (59° to 77°F). Keep out of reach of children. Distributed by: Bausch + Lomb, a division of Bausch Health US, LLC Bridgewater, NJ 08807 USA Manufactured by: Bausch Health Companies Inc. Laval, Quebec H7L 4A8, Canada © 2019 Bausch & Lomb Incorporated or its affiliates Revised: May 2019 9681901
Abbreviated New Drug Application
FLUNISOLIDE- FLUNISOLIDE SOLUTION BAUSCH & LOMB INCORPORATED ---------- FLUNISOLIDE NASAL SOLUTION, USP 0.025% RX ONLY FOR INTRANASAL USE ONLY DESCRIPTION Flunisolide Nasal Solution, USP 0.025% is intended for administration as a spray to the nasal mucosa. Flunisolide, the active component of Flunisolide Nasal Solution, is an anti- inflammatory steroid. Flunisolide is represented by the following structural formula: C H FO • 1/2H O Mol. Wt. 443.52 Chemical Name: 24 31 6 2 6α-fluoro-11β,16α,17,21-tetrahydroxypregna-1,4-diene-3,20-dione cyclic 16,17-acetal with acetone (USAN). Flunisolide is a white to creamy white crystalline powder. It is soluble in acetone, sparingly soluble in chloroform, slightly soluble in methanol, and practically insoluble in water. It has a melting point of about 245°C. After initial priming (5 to 6 sprays), each spray of the unit delivers a metered droplet spray of 100 mg formulation containing 25 mcg of flunisolide. The size of the droplets produced by the unit is in excess of 8 microns to facilitate deposition on the nasal mucosa. The contents of one nasal spray bottle delivers 200 sprays. EACH ML CONTAINS: _ACTIVE:_Flunisolide 0.25 mg (0.025%); _INACTIVES:_Propylene Glycol, Polyethylene Glycol 3350, Butylated Hydroxyanisole, Edetate Disodium, Sodium Citrate, Citric Acid, and Purified Water. Sodium Hydroxide and/or Hydrochloric Acid may be added to adjust pH (5.1–5.4). _PRESERVATIVE:_Benzalkonium Chloride 0.01%. CLINICAL PHARMACOLOGY Flunisolide has demonstrated potent glucocorticoid and weak mineralocorticoid activity in classical animal test systems. As a glucocorticoid, it is several hundred times more potent than the cortisol standard. Clinical studies with flunisolide have shown therapeutic activity on nasal mucous membranes with minimal evidence of systemic activity at the recommended doses. A study in approximately 100 patients that compared the recommended dose of Flunisolide Nasal Solution with an oral dose providing equivalent systemic amounts of flunisolide has shown Izlasiet visu dokumentu