Depakote

Active Ingredient(s): Valproic Acid, Divalproex Sodium
FDA Approved: * March 10, 1983
Pharm Company: * ABBOTT
Category: Migraine / Tension Headache

Valproate (VPA) and its valproic acid, sodium valproate, and valproate semisodium forms are medications primarily used to treat epilepsy and bipolar disorder and prevent migraine headaches.[2] They are useful for the prevention of seizures in those with absence seizures, partial seizures, and generalized seizures.[2] They can be given intravenously or by mouth, and the tablet forms exist in both long- and short-acting formulations.[2] Common sid... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
101 Discussions

Dosage List

Depakote a;NT
Depakote 125 mg Enteric Coated Tablet
NDC: 0074-6212
Labeler:
Abbvie Inc.
Depakote a;NR
Depakote 250 mg Enteric Coated Tablet
NDC: 0074-6214
Labeler:
Abbvie Inc.
Depakote a;NS
Depakote 500 mg Enteric Coated Tablet
NDC: 0074-6215
Labeler:
Abbvie Inc.
Depakote a;NR
Depakote 250 mg Oral Tablet, Delayed Release
NDC: 24236-225
Labeler:
Remedyrepack Inc.
Depakote a;NS
Depakote 500 mg Oral Tablet, Delayed Release
NDC: 24236-771
Labeler:
Remedyrepack Inc.
Depakote a;NR
Depakote 250 mg Enteric Coated Tablet
NDC: 49999-941
Labeler:
Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
Depakote a;NS
Depakote 500 mg Oral Tablet, Delayed Release
NDC: 52125-988
Labeler:
Remedyrepack Inc.
Depakote a;NR
Depakote 250 mg Oral Tablet, Delayed Release
NDC: 61786-125
Labeler:
Remedyrepack Inc.
Depakote a;NR
Depakote 250 mg Oral Tablet, Delayed Release
NDC: 70518-1454
Labeler:
Remedyrepack Inc.
Depakote a;NS
Depakote 500 mg Oral Tablet, Delayed Release
NDC: 70518-1456
Labeler:
Remedyrepack Inc.
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