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a HF (Divalproex Sodium Extended-Release 250 mg)

Pill with imprint a HF is White, Elliptical/Oval and has been identified as Divalproex Sodium Extended-Release 250 mg. It is supplied by Zydus Pharmaceuticals USA Inc.

Divalproex sodium is used in the treatment of bipolar disorder; mania; epilepsy; migraine prevention and belongs to the drug class fatty acid derivative anticonvulsants. When treating epilepsy and manic episodes associated with bipolar disorder: There is positive evidence of human fetal risk during pregnancy. When treating migraine: Not for use in pregnancy. Divalproex sodium 250 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for a HF

Divalproex Sodium Extended-Release

a HF
250 mg
Prescription only
Drug Class
Fatty acid derivative anticonvulsants
Pregnancy Category
D - Positive evidence of risk - When treating epilepsy and manic episodes associated with bipolar disorder, X - Not for use in pregnancy - When treating migraine
CSA Schedule
Not a controlled drug
Labeler / Supplier
Zydus Pharmaceuticals USA Inc.
Inactive Ingredients
titanium dioxide, lactose, silicon dioxide, potassium sorbate, propylene glycol, polyethylene glycol, FD&C Blue No. 1, hypromelloses, microcrystalline cellulose, triacetin

Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code Labeler / Repackager
68382-0314 (Discontinued) Zydus Pharmaceuticals (USA) Inc.
00074-3826 Abbott Laboratories
54868-5525 (Discontinued) Physicians Total Care Inc. (repackager)
67544-0904 Prepak Systems Inc. (repackager)
35356-0345 Lake Erie Medical and Surgical Supply (repackager)
49999-0941 (Discontinued) Lake Erie Medical and Surgical Supply (repackager)

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.