U-S 182 Pill - pink oval, 19mm
Pill with imprint U-S 182 is Pink, 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; Mania; Epilepsy; Migraine Prevention; 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 182
Divalproex Sodium Delayed-Release
- Imprint
- U-S 182
- Strength
- 500 mg
- Color
- Pink
- Size
- 19.00 mm
- Shape
- 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
- National Drug Code (NDC)
- 00245-0182 (Discontinued)
- 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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- Drug class: fatty acid derivative anticonvulsants
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Professional resources
- Divalproex Capsules prescribing information
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- Divalproex Extended Release (FDA)
- Divalproex Sprinkle (FDA)
Other brands
Depakote, Depakote ER, Depakote Sprinkles
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
