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; migraine prevention; epilepsy; 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 Substances Act (CSA).

Images for Watson 667

Divalproex Sodium Delayed Release

Imprint:

Watson 667

Strength:

500 mg

Color:

Red

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:

Watson Laboratories, Inc.

National Drug Code (NDC):

62037-0667

Inactive Ingredients:

candelilla wax
cellacefate
silicon dioxide colloidal
croscarmellose sodium
dextrates
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
triacetin
aluminum oxide
Note: Inactive ingredients may vary.

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