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 (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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