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; hyperekplexia; epilepsy (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).
- 93 7441
- 500 mg
- 19.00 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 (6 mPa.s)
hypromellose phthalate (31% phthalate, 40 cst)
polyethylene glycol 3350
ferric oxide red
ferric oxide yellow
More about divalproex sodium
- Divalproex delayed-release tablets
- Divalproex extended-release tablets
- Divalproex sprinkle capsules
- Divalproex sodium
- Divalproex sodium (Advanced Reading)
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