NDC 29300-0140-01
Divalproex Sodium 500 mg/1 TABLET, DELAYED RELEASE
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NDC
29300-0140-01
Generic Name
Divalproex Sodium
Brand Name
Divalproex Sodium
Strength
500 mg/1
Dosage Form
TABLET, DELAYED RELEASE
Route
ORAL
Package Size
—
Labeler
Unichem Pharmaceuticals (USA), Inc.
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Divalproex sodium is an anti-epileptic drug indicated for: Treatment of manic episodes associated with bipolar disorder ( 1.1 ) Monotherapy and adjunctive therapy of complex partial seizures and simple and complex absence seizures; adjunctive therapy in patients with multiple seizure types that include absence seizures ( 1.2 ) Prophylaxis of migraine headaches ( 1.3 ) 1.1 Mania Divalproex sodium delayed-release tablets are valproate and is indicated for the treatment of t…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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