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AN 757 (Divalproex Sodium Extended-Release 500 mg)

Pill with imprint AN 757 is White, Capsule-shape and has been identified as Divalproex Sodium Extended-Release 500 mg. It is supplied by Amneal 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 AN 757

Divalproex sodium extended-release 500 mg AN 757
Divalproex sodium extended-release 500 mg AN 757  Front
Divalproex sodium extended-release 500 mg AN 757  Back
Divalproex sodium extended-release 500 mg AN 757
Divalproex sodium extended-release 500 mg AN 757

Divalproex Sodium Extended-Release

Imprint
AN 757
Strength
500 mg
Color
White
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
Amneal Pharmaceuticals
National Drug Code (NDC)
65162-0757

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Further information

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