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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; migraine prevention; mania; borderline personality disorder; epilepsy (and more), 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 Substance Act (CSA).

Images for 692

Divalproex sodium extended-release

Imprint:
692
Strength:
500 mg
Color:
White
Size:
6.00 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
Inactive Ingredients:
silicon dioxide
copovidone
calcium phosphate dihydrate dibasic
hydrogenated cottonseed oil
hypromellose
polyethylene glycol
polyvinyl alcohol
magnesium silicate
titanium dioxide
microcrystalline cellulose
stearic acid
xanthan gum
Note: Inactive ingredients may vary.

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Disclaimer: Every effort has been made to ensure that the information provided is accurate, up-to-date, and complete, but no guarantee is made to that effect. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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