U-S 500 (Divalproex Sodium Delayed-Release 500 mg)
Pill with imprint U-S 500 is Pink, Capsule-shape and has been identified as Divalproex Sodium Delayed-Release 500 mg. It is supplied by Upsher-Smith Laboratories, Inc.
Divalproex sodium is used in the treatment of bipolar disorder; mania; epilepsy; migraine prevention 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 U-S 500
- U-S 500
- 500 mg
- 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
- Upsher-Smith Laboratories, Inc.
- National Drug Code (NDC)
- Inactive Ingredients
methacrylic acid - ethyl acrylate copolymer (1:1) type a,
sodium lauryl sulfate,
FD&C Red No. 40
Note: Inactive ingredients may vary.
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More about divalproex sodium
- Side effects
- Drug interactions
- Dosage information
- During pregnancy or Breastfeeding
- Reviews (461)
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- Drug class: fatty acid derivative anticonvulsants
- Drug Information
- Divalproex sodium (Advanced Reading)
- Divalproex Sprinkle Capsules
- Divalproex Long-Acting Tablets
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