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798 (Divalproex sodium delayed-release 500 mg)

Pill imprint 798 has been identified as Divalproex sodium delayed-release 500 mg.

Divalproex sodium is used in the treatment of bipolar disorder; mania; migraine prevention; hyperekplexia; epilepsy (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 classified as a Schedule N controlled substance under the Controlled Substance Act (CSA).

Divalproex sodium delayed-release 500 mg 798
Divalproex sodium delayed-release
500 mg
19.00 mm
Elliptical / Oval
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:
N - Not a controlled drug
Sun Pharmaceuticals
National Drug Code (NDC):
Inactive Ingredients:
silicon dioxide
corn starch
povidone k30
titanium dioxide
methacrylic acid - ethyl acrylate copolymer (1:1) type a
magnesium silicate
triethyl citrate
sodium bicarbonate
sodium lauryl sulfate
D&C Red No. 30
FD&C Blue No. 2
ferric oxide red

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