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U-S 500 (Divalproex Sodium Delayed-Release 500 mg)

Pill with imprint U-S 500 is Pink, Capsule-shape and has been identified as Divalproex Sodium Delayed-Release 500 mg. It is supplied by Upsher-Smith Laboratories, Inc..

Divalproex sodium is used in the treatment of bipolar disorder; migraine prevention; mania; 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 Substances Act (CSA).

Images for U-S 500

Divalproex sodium delayed-release 500 mg U-S 500
Divalproex sodium delayed-release 500 mg U-S 500
Divalproex sodium delayed-release 500 mg U-S 500

Divalproex Sodium Delayed-Release

Imprint:
U-S 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:
Upsher-Smith Laboratories, Inc.
National Drug Code (NDC):
00832-7124

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Further information

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

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