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692 (Divalproex Sodium Extended-Release 500 mg)

Pill with imprint 692 is White, Capsule-shape and has been identified as Divalproex Sodium Extended-Release 500 mg. It is supplied by Global Pharmaceuticals.

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 692

Divalproex sodium extended-release 500 mg 692

Divalproex Sodium Extended-Release

Imprint
692
Strength
500 mg
Color
White
Size
21.00 mm
Shape
Capsule-shape
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
Global Pharmaceuticals
National Drug Code (NDC)
00115-6922
Inactive Ingredients
silicon dioxide, copovidone, calcium phosphate dihydrate dibasic, hydrogenated cottonseed oil, hypromelloses, polyethylene glycol, magnesium silicate, titanium dioxide, microcrystalline cellulose, stearic acid, xanthan gum

Note: Inactive ingredients may vary.

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Further information

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