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93 7439 (Divalproex sodium delayed-release 125 mg)

Pill imprint 93 7439 has been identified as Divalproex sodium delayed-release 125 mg.

Divalproex sodium is used in the treatment of bipolar disorder; mania; migraine prevention; epilepsy; borderline personality disorder (and more), 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 Substance Act (CSA).

Divalproex sodium delayed-release 125 mg 93 7439
Discount Card Promo
Divalproex sodium delayed-release
93 7439
125 mg
12.00 mm
Elliptical / Oval
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
Teva Pharmaceuticals USA
National Drug Code (NDC):
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
polyvinyl alcohol
povidone k30
corn starch
propylene glycol
silicon dioxide
magnesium silicate
titanium dioxide
triethyl citrate
D&C Yellow No. 10
aluminum oxide
FD&C Red No. 40
FD&C Yellow No. 6

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