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93 7441 (Divalproex Sodium Delayed-Release 500 mg)

Pill with imprint 93 7441 is Orange, Elliptical / Oval and has been identified as Divalproex Sodium Delayed-Release 500 mg. It is supplied by Teva Pharmaceuticals USA.

Divalproex sodium is used in the treatment of bipolar disorder; mania; migraine prevention; epilepsy 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 93 7441

Divalproex Sodium Delayed-Release

Imprint:
93 7441
Strength:
500 mg
Color:
Orange
Size:
19.00 mm
Shape:
Elliptical / Oval
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:
Teva Pharmaceuticals USA
National Drug Code (NDC):
00093-7441
Inactive Ingredients:

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.

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