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U-S 500 Pill - pink capsule/oblong, 19mm

Pill with imprint U-S 500 is Pink, Capsule/Oblong 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; Migraine Prevention; Epilepsy; Seizures 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

Divalproex sodium delayed-release 500 mg U-S 500
Divalproex sodium delayed-release 500 mg U-S 500
Divalproex sodium delayed-release 500 mg U-S 500
Divalproex sodium delayed-release 500 mg U-S 500

Divalproex Sodium Delayed-Release

Imprint
U-S 500
Strength
500 mg
Color
Pink
Size
19.00 mm
Shape
Capsule/Oblong
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.
National Drug Code (NDC)
00832-7124
Inactive Ingredients
methacrylic acid - ethyl acrylate copolymer (1:1) type a, 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.