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; mania; migraine prevention; epilepsy; cyclothymic disorder (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 U-S 182 (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
- 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
Divalproex sodium delayed-release is associated with the treatment of:
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