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U-S 182 (Divalproex Sodium Delayed-Release 500 mg)

Pill with imprint U-S 182 is Pink, Elliptical / Oval 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; epilepsy; mania; migraine prevention; borderline personality disorder (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 Substances Act (CSA).

Images for U-S 182

Divalproex Sodium Delayed-Release

Imprint:
U-S 182
Strength:
500 mg
Color:
Pink
Size:
19.00 mm
Shape:
Elliptical / Oval
Availability:
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
Inactive Ingredients:
methacrylic acid - ethyl acrylate copolymer (1:1) type a
povidone
corn starch
silicon dioxide
sodium bicarbonate
sodium lauryl sulfate
magnesium silicate
triethyl citrate
titanium dioxide
vanillin
FD&C Red No. 40
Note: Inactive ingredients may vary.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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