93 7441 (Divalproex sodium delayed-release 500 mg)

Pill imprint 93 7441 has been identified as Divalproex sodium delayed-release 500 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 500 mg is not a controlled substance under the Controlled Substance Act (CSA).

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

Manufacturer:

Teva Pharmaceuticals USA

National Drug Code (NDC):

00093-7441

Inactive Ingredients:

ammonia
crospovidone
hypromellose 2910 (6 mPa.s)
hypromellose phthalate (31% phthalate, 40 cst)
ferrosoferric oxide
lactose monohydrate
magnesium stearate
microcrystalline cellulose
polyethylene glycol 3350
polyvinyl alcohol
povidone k30
corn starch
propylene glycol
shellac
silicon dioxide
magnesium silicate
titanium dioxide
triethyl citrate
ferric oxide red
ferric oxide yellow
triacetin

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