93 7441 Pill - orange oval, 19mm
Pill with imprint 93 7441 is Orange, 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; 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 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
- 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 (Discontinued)
- Inactive Ingredients
-
hypromellose 2910 (6 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,
ferric oxide red,
ferric oxide yellow,
triacetin
Note: Inactive ingredients may vary.
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Patient resources
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Professional resources
- Divalproex Capsules prescribing information
- Divalproex Delayed Release (FDA)
- 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.