U-S 182 (Divalproex sodium delayed-release 500 mg)
Pill imprint U-S 182 has been identified as Divalproex sodium delayed-release 500 mg.
Divalproex sodium is used in the treatment of bipolar disorder; migraine prevention; mania; 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 subject to the Controlled Substances Act.
See also related documents.
Images for U-S 182
- 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:
- N - Not a controlled drug
- 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
More about divalproex sodium
- Divalproex delayed-release tablets
- Divalproex extended-release tablets
- Divalproex sprinkle capsules
- Divalproex sodium
- Divalproex sodium (Advanced Reading)
Related treatment guides
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