W975 (Divalproex 500 mg)

Pill imprint W975 has been identified as Divalproex sodium delayed-release 500 mg.

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 Substance Act (CSA).

Divalproex sodium delayed-release

Imprint:

W975

Strength:

500 mg

Color:

White

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

Manufacturer:

Wockhardt USA

National Drug Code (NDC):

64679-0975

Inactive Ingredients:

silicon dioxide
microcrystalline cellulose
corn starch
povidone
croscarmellose sodium
glyceryl behenate
magnesium silicate
hypromelloses
polyethylene glycol
polyvinyl alcohol
polysorbate 80
methacrylic acid - ethyl acrylate copolymer (1:1) type a
triethyl citrate
sodium bicarbonate
sodium lauryl sulfate
dimethicone
titanium dioxide

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