Mometasone Furoate Solution

Mometasone Furoate Solution Manufacturers

• Perrigo New York Inc
  

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  Mometasone Furoate Solution | Aplicare, Inc.

  

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  Directions apply locally as needed

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• Physicians Total Care, Inc.
  

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  Mometasone Furoate Solution | Physicians Total Care, Inc.

  

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  Apply a few drops of Mometasone Furoate Lotion (Mometasone Furoate Topical Solution USP 0.1%) to the affected areas once daily and massage lightly until it disappears. For the most effective and economical use, hold nozzle of the bottle very close to the affected areas and gently squeeze. Since safety and efficacy of Mometasone Furoate Lotion (Mometasone Furoate Topical Solution USP 0.1%) have not been established in pediatric patients below 12 years of age, its use in this age group is not recommended. (see PRECAUTIONS -Pediatric Use). As with other corticosteroids, therapy should be discontinued when control is achieved. If no improvement is seen within 2 weeks, reassessment of diagnosis may be necessary. Mometasone Furoate Lotion (Mometasone Furoate Topical Solution USP 0.1%) should not be used with occlusive dressings unless directed by a physician. Mometasone Furoate Lotion (Mometasone Furoate Topical Solution USP 0.1%) should not be applied in the diaper area if the patient requires diapers or plastic pants as these garments may constitute occlusive dressing.

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• E. Fougera & Co., A Division Of Fougera Pharmaceuticals Inc.
  

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  Mometasone Furoate Solution | Unit Dose Services

  

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  Adult:

  The maximum recommended single dose of lidocaine hydrochloride oral topical solution, 2% (viscous) for healthy adults should be such that the dose of lidocaine HCl does not exceed 4.5 mg/kg or 2 mg/lb body weight and does not in any case exceed a total of 300 mg.

  For symptomatic treatment of irritated or inflamed mucous membranes of the mouth and pharynx, the usual adult dose is one 15 mL tablespoonful undiluted. For use in the mouth, the solution should be swished around in the mouth and spit out. For use in the pharynx, the undiluted solution should be gargled and may be swallowed. This dose should not be administered at intervals of less than three hours, and not more than eight doses should be given in a 24-hour period.

  The dosage should be adjusted commensurate with the patient's age, weight, and physical condition (see ). PRECAUTIONS

  Pediatric:

  Care must be taken to ensure correct dosage in all pediatric patients as there have been cases of overdose due to inappropriate dosing.

  It is difficult to recommend a maximum dose of any drug for children since this varies as a function of age and weight. For children over 3 years of age who have a normal lean body mass and normal body development, the maximum dose is determined by the child's weight or age. For example: in a child of 5 years weighing 50 lbs., the dose of lidocaine hydrochloride should not exceed 75 to 100 mg (3.7 to 5 mL of lidocaine hydrochloride oral topical solution 2% (viscous)).

  For infants and in children under 3 years of age, the solution should be accurately measured and no more than 1.2 mL be applied to the immediate area with a cotton-tipped applicator. Wait at least 3 hours before giving the next dose; a maximum of four doses may be given in a 12-hour period. Lidocaine hydrochloride oral topical solution 2% (viscous) should only be used if the underlying condition requires treatment with a volume of product that is less than or equal to 1.2 mL.

  Adult:

  The maximum recommended single dose of lidocaine hydrochloride oral topical solution, 2% (viscous) for healthy adults should be such that the dose of lidocaine HCl does not exceed 4.5 mg/kg or 2 mg/lb body weight and does not in any case exceed a total of 300 mg.

  For symptomatic treatment of irritated or inflamed mucous membranes of the mouth and pharynx, the usual adult dose is one 15 mL tablespoonful undiluted. For use in the mouth, the solution should be swished around in the mouth and spit out. For use in the pharynx, the undiluted solution should be gargled and may be swallowed. This dose should not be administered at intervals of less than three hours, and not more than eight doses should be given in a 24-hour period.

  The dosage should be adjusted commensurate with the patient's age, weight, and physical condition (see ). PRECAUTIONS

  Pediatric:

  Care must be taken to ensure correct dosage in all pediatric patients as there have been cases of overdose due to inappropriate dosing.

  It is difficult to recommend a maximum dose of any drug for children since this varies as a function of age and weight. For children over 3 years of age who have a normal lean body mass and normal body development, the maximum dose is determined by the child's weight or age. For example: in a child of 5 years weighing 50 lbs., the dose of lidocaine hydrochloride should not exceed 75 to 100 mg (3.7 to 5 mL of lidocaine hydrochloride oral topical solution 2% (viscous)).

  For infants and in children under 3 years of age, the solution should be accurately measured and no more than 1.2 mL be applied to the immediate area with a cotton-tipped applicator. Wait at least 3 hours before giving the next dose; a maximum of four doses may be given in a 12-hour period. Lidocaine hydrochloride oral topical solution 2% (viscous) should only be used if the underlying condition requires treatment with a volume of product that is less than or equal to 1.2 mL.

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• Taro Pharmaceuticals U.s.a., Inc.
  

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  Mometasone Furoate Solution | Mylan Pharmaceuticals Inc.

  

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  Use the lowest effective dose for the patient.

  2.1 Dosage in Adults

  The recommended starting dose is 1 mg. Dosing can be raised to 2 mg or 3 mg if clinically indicated. In some patients, the higher morning blood levels of eszopiclone tablets following use of the 2 mg or 3 mg dose increase the risk of next day impairment of driving and other activities that require full alertness [see Warnings and Precautions (5.1)]. The total dose of eszopiclone tablets should not exceed 3 mg, once daily immediately before bedtime [see Warnings and Precautions (5.6)].

  2.2 Geriatric or Debilitated Patients

  The total dose of eszopiclone tablets should not exceed 2 mg in elderly or debilitated patients.

  2.3 Patients with Severe Hepatic Impairment, or Taking Potent CYP3A4 Inhibitors

  In patients with severe hepatic impairment, or in patients coadministered eszopiclone tablets with potent CYP3A4 inhibitors, the total dose of eszopiclone tablets should not exceed 2 mg [see Warnings and Precautions (5.7)].

  2.4 Use with CNS Depressants

  Dosage adjustments may be necessary when eszopiclone tablets are combined with other CNS depressant drugs because of the potentially additive effects [see Warnings and Precautions (5.1)].

  2.5 Administration with Food

  Taking eszopiclone tablets with or immediately after a heavy, high-fat meal results in slower absorption and would be expected to reduce the effect of eszopiclone tablets on sleep latency [see Clinical Pharmacology (12.3)].

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