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93 7440 (Divalproex Sodium Delayed-Release 250 mg)

Pill with imprint 93 7440 is Orange, Elliptical / Oval and has been identified as Divalproex Sodium Delayed-Release 250 mg. It is supplied by Teva Pharmaceuticals USA.

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 250 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for 93 7440

Divalproex sodium delayed-release 250 mg 93 7440
Divalproex sodium delayed-release 250 mg 93 7440
Divalproex sodium delayed-release 250 mg 93 7440  Front
Divalproex sodium delayed-release 250 mg 93 7440  Back

Divalproex Sodium Delayed-Release

Imprint
93 7440
Strength
250 mg
Color
Orange
Size
15.00 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)
00093-7440
Inactive Ingredients
hypromellose 2910 (15 mPa.s), hypromellose phthalate (31% phthalate, 40 cst), ferrosoferric oxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol 3350, polyethylene glycol 4000, povidone k30, corn starch, propylene glycol, shellac, silicon dioxide, magnesium silicate, titanium dioxide, triethyl citrate, FD&C Blue No. 2, indigotindisulfonate sodium, ferric oxide red, ferric oxide yellow

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.