93 7439 Pill - orange oval, 12mm
Pill with imprint 93 7439 is Orange, Oval and has been identified as Divalproex Sodium Delayed-Release 125 mg. It is supplied by Teva Pharmaceuticals USA.
Divalproex sodium is used in the treatment of Bipolar Disorder; Mania; Migraine Prevention; Seizures; 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 125 mg is not a controlled substance under the Controlled Substances Act (CSA).
Images for 93 7439
Divalproex Sodium Delayed-Release
- Imprint
- 93 7439
- Strength
- 125 mg
- Color
- Orange
- Size
- 12.00 mm
- Shape
- 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)
- 00093-7439 (Discontinued)
- 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,
D&C Yellow No. 10,
FD&C Red No. 40,
FD&C Yellow No. 6
Note: Inactive ingredients may vary.
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Professional resources
- Divalproex Capsules prescribing information
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- Divalproex Sprinkle (FDA)
Other brands
Depakote, Depakote ER, Depakote Sprinkles
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.