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; migraine prevention; mania; epilepsy; hyperekplexia (and more), and belongs to the drug class fatty acid derivative anticonvulsants. There is positive evidence of human fetal risk during pregnancy. Divalproex sodium 500 mg is not subject to the Controlled Substances Act.
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Images for 93 7441 (Divalproex sodium delayed-release 500 mg)
- 500 mg
- 19.00 mm
- Elliptical / Oval
- Prescription only
- Drug Class:
- Fatty acid derivative anticonvulsants
- Pregnancy Category:
- D - Positive evidence of risk
- CSA Schedule:
- N - 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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