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AN 757 Pill - white capsule/oblong, 21mm

Pill with imprint AN 757 is White, Capsule/Oblong 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; Migraine Prevention; Epilepsy; Seizures 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
Size
21.00 mm
Shape
Capsule/Oblong
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
Inactive Ingredients
ammonia, methacrylic acid - methyl methacrylate copolymer (1:1), hypromelloses, ferrosoferric oxide, isopropyl alcohol, lactose monohydrate, polyethylene glycol, magnesium stearate, microcrystalline cellulose, butyl alcohol, propylene glycol, shellac, silicon dioxide, magnesium silicate, titanium dioxide

Note: Inactive ingredients may vary.

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Further information

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