U-S 250 Pill: peach, capsule/oblong, 15mm
The pill with imprint U-S 250 (Peach, Capsule/Oblong, 15mm) has been identified as Divalproex Sodium Delayed-Release 250 mg and is used for Bipolar Disorder, Mania, Migraine Prevention, Seizures, and Epilepsy. It belongs to the drug class fatty acid derivative anticonvulsants and is not a controlled substance.
Images for U-S 250
Divalproex Sodium Delayed-Release
- Imprint
- U-S 250
- Strength
- 250 mg
- Color
- Peach
- Size
- 15.00 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)
- 00832-7123
- 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 Yellow No. 6,
ferric oxide red
Note: Inactive ingredients may vary.
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Depakote, Depakote ER, Depakote Sprinkles
Professional resources
- Divalproex Capsules prescribing information
- Divalproex Delayed Release (FDA)
- Divalproex Delayed Release Tablets (FDA)
- Divalproex Extended Release (FDA)
- Divalproex Sprinkle (FDA)
Other brands
Depakote, Depakote ER, Depakote Sprinkles
Related treatment guides
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.