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UL 500 (Divalproex Sodium Delayed Release 500 mg)

Pill with imprint UL 500 is Pink, Capsule-shape and has been identified as Divalproex Sodium Delayed Release 500 mg. It is supplied by Unichem Pharmaceuticals (USA), Inc..

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 UL 500

Divalproex sodium delayed release 500 mg UL 500
Divalproex sodium delayed release 500 mg UL 500  Front
Divalproex sodium delayed release 500 mg UL 500  Back
Divalproex sodium delayed release 500 mg UL 500
Divalproex sodium delayed release 500 mg UL 500

Divalproex Sodium Delayed Release

Imprint
UL 500
Strength
500 mg
Color
Pink
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
Labeler / Supplier
Unichem Pharmaceuticals (USA), Inc.
National Drug Code (NDC)
29300-0140

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Further information

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