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798 (Divalproex Sodium Delayed-Release 500 mg)

Pill with imprint 798 is Pink, Elliptical / Oval and has been identified as Divalproex Sodium Delayed-Release 500 mg. It is supplied by Sun Pharmaceuticals.

Divalproex sodium is used in the treatment of bipolar disorder; mania; epilepsy; migraine prevention 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 798

Divalproex sodium delayed-release 500 mg 798
Divalproex sodium delayed-release 500 mg 798
Divalproex sodium delayed-release 500 mg 798  Front
Divalproex sodium delayed-release 500 mg 798  Back
Divalproex sodium delayed-release 500 mg 798
Divalproex sodium delayed-release 500 mg 798

Divalproex Sodium Delayed-Release

Imprint
798
Strength
500 mg
Color
Pink
Size
19.00 mm
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
Sun Pharmaceuticals
National Drug Code (NDC)
62756-0798
Inactive Ingredients
silicon dioxide, corn starch, povidone, hypromelloses, titanium dioxide, triacetin, methacrylic acid - ethyl acrylate copolymer (1:1) type a, triethyl citrate, sodium bicarbonate, sodium lauryl sulfate, D&C Red No. 30, FD&C Blue No. 2, shellac, ferrosoferric oxide, butyl alcohol, propylene glycol, ammonia, ferric oxide red, magnesium silicate

Note: Inactive ingredients may vary.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.