modafinil 100 mg

1 INDICATIONS AND USAGE Modafinil tablets, USP are indicated to improve wakefulness in adult patients with excessive sleepiness associated with narcolepsy, obstructive sleep apnea (OSA), or shift work disorder (SWD). Limitations of Use In OSA, modafinil tablets, USP are indicated to treat excessive sleepiness and not as treatment for the underlying obstruction. If continuous positive airway pressure (CPAP) is the treatment of choice for a patient, a maximal effort to treat with CPAP for an adequate period of time should be made prior to initiating and during treatment with modafinil tablets, USP for excessive sleepiness. Modafinil tablets, USP are indicated to improve wakefulness in adult patients with excessive sleepiness associated with narcolepsy, obstructive sleep apnea (OSA), or shift work disorder (SWD). (1) Limitations of Use In OSA, modafinil tablets, USP are indicated to treat excessive sleepiness and not as treatment for the underlying obstruction.

NuCare Pharmaceuticals,Inc.

FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] nausea` `[3] fatigue` `[4] off label use` `[5] diarrhoea` `[6] dyspnoea` `[7] pain` `[8] headache` `[9] vomiting` `[10] dizziness`

2 years ago

OVAL WHITE J 41

16 HOW SUPPLIED/STORAGE AND HANDLING 16.1 How Supplied Modafinil Tablets USP, 100 mg are white to off-white, capsule-shaped, uncoated tablets, debossed with 41 on one side and J on the other side. NDC 68071-5121-3 BOTTLES OF 30 16.2 Storage Store at 20 o to 25 o C (68 o to 77 o F). [See USP Controlled Room Temperature.]

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modafinil 100 mg

FDA Reported Adverse Reactions [1] drug ineffective [2] nausea [3] fatigue [4] off label use [5] diarrhoea [6] dyspnoea [7] pain [8] headache [9] vomiting [10] dizziness

OVAL WHITE J 41

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FDA Reported Adverse Reactions
`[1] drug ineffective` `[2] nausea` `[3] fatigue` `[4] off label use` `[5] diarrhoea` `[6] dyspnoea` `[7] pain` `[8] headache` `[9] vomiting` `[10] dizziness`