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Watson 667 (Divalproex sodium delayed release 500 mg)

Pill with imprint Watson 667 is Red, Elliptical / Oval and has been identified as Divalproex sodium delayed release 500 mg. It is supplied by Watson Laboratories, Inc..

Divalproex sodium is used in the treatment of bipolar disorder; mania; epilepsy; migraine prevention; borderline personality disorder (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 Watson 667

Divalproex sodium delayed release

Watson 667
500 mg
Elliptical / Oval
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:
Watson Laboratories, Inc.
Inactive Ingredients:
candelilla wax
silicon dioxide colloidal
croscarmellose sodium
FD&C Red No. 40
hydroxypropyl cellulose
hypromellose 2910 (15 mPa.s)
ferrosoferric oxide
lactose monohydrate
magnesium stearate
microcrystalline cellulose
propylene glycol
silicon dioxide
titanium dioxide
aluminum oxide
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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