NDC 69452-0343-13
Modafinil 200 mg/1 TABLET
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NDC
69452-0343-13
Generic Name
Modafinil
Brand Name
Modafinil
Strength
200 mg/1
Dosage Form
TABLET
Route
ORAL
Package Size
—
Labeler
Bionpharma Inc.
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Modafinil tablets 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 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…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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