691 (Divalproex Sodium Extended-Release 250 mg)

This pill with imprint "691" is White, Capsule-shape and has been identified as Divalproex sodium extended-release 250 mg. It is manufactured by Global Pharmaceuticals.

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 250 mg is not a controlled substance under the Controlled Substance Act (CSA).

Divalproex sodium extended-release

Imprint:

691

Strength:

250 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

Manufacturer:

Global Pharmaceuticals

National Drug Code (NDC):

00115-6911

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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