a HC (Divalproex Sodium Extended-Release 500 mg)

Pill with imprint a HC is Gray, Elliptical/Oval and has been identified as Divalproex Sodium Extended-Release 500 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 500 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for a HC

Divalproex Sodium Extended-Release

Imprint: a HC
Strength: 500 mg
Color: Gray
Shape: Elliptical/Oval
Availability: 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: lactose, silicon dioxide, potassium sorbate, propylene glycol, titanium dioxide, polyethylene glycol, FD&C Blue No. 1, hypromelloses, microcrystalline cellulose, triacetin, ferric oxide red, polydextrose
Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code	Labeler / Repackager
68382-0315 (Discontinued)	Zydus Pharmaceuticals (USA) Inc.
00074-7126	Abbott Laboratories
54868-4959 (Discontinued)	Physicians Total Care Inc. (repackager)
49999-0875	Lake Erie Medical and Surgical Supply (repackager)
55289-0404	PDRX Pharmaceuticals Inc. (repackager)