R531 (Divalproex sodium delayed-release 500 mg)

Pill imprint R531 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:

R531

Strength:

500 mg

Color:

Pink

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:

Dr. Reddy’s Laboratories Inc.

National Drug Code (NDC):

55111-0531

Inactive Ingredients:

acetone
hypromellose
hypromellose phthalate (31% phthalate, 40 cst)
isopropyl alcohol
methylene chloride
microcrystalline cellulose
povidone
corn starch
silicon dioxide
magnesium silicate
titanium dioxide
vanillin
shellac
ferrosoferric oxide
butyl alcohol
soya lecithin
ferric oxide red

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