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NDC 29300-0138-05

Divalproex Sodium 125 mg/1 TABLET, DELAYED RELEASE

Unichem Pharmaceuticals (USA), Inc.

Available — 2-Day Shipping
NDC
29300-0138-05
Generic Name
Divalproex Sodium
Brand Name
Divalproex Sodium
Strength
125 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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Other Divalproex Sodium NDC Codes

55111-0532-05125 mg/1CAPSULE, DELAYED RELEASE
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55111-0532-01125 mg/1CAPSULE, DELAYED RELEASE
2-Day
29300-0138-01125 mg/1TABLET, DELAYED RELEASE
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29300-0139-01250 mg/1TABLET, DELAYED RELEASE
2-Day
29300-0139-05250 mg/1TABLET, DELAYED RELEASE
2-Day

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