NDC 68180-0261-02
Divalproex sodium 500 mg/1 TABLET, EXTENDED RELEASE
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NDC
68180-0261-02
Generic Name
Divalproex sodium
Brand Name
Divalproex sodium
Strength
500 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
Lupin Pharmaceuticals, Inc.
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Divalproex sodium extended-release tablets are indicated for: Acute treatment of manic or mixed episodes associated with bipolar disorder, with or without psychotic features ( 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 extended-release tablets…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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