Skip to Content

UL 125 (Divalproex Sodium Delayed Release 125 mg)

Pill with imprint UL 125 is Orange, Capsule-shape and has been identified as Divalproex Sodium Delayed Release 125 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 125 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for UL 125

Divalproex sodium delayed release 125 mg UL 125
Divalproex sodium delayed release 125 mg UL 125
Divalproex sodium delayed release 125 mg UL 125

Divalproex Sodium Delayed Release

Imprint
UL 125
Strength
125 mg
Color
Orange
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)
29300-0138

Get help with Imprint Code FAQs.

Related Images for "UL 125"

Further information

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