THIS END UP RDY 532 Pill - blue & white capsule/oblong, 19mm
Pill with imprint THIS END UP RDY 532 is Blue & White, Capsule/Oblong and has been identified as Divalproex Sodium Delayed-Release (Sprinkle) 125 mg. It is supplied by Dr. Reddy’s Laboratories Inc.
Divalproex sodium is used in the treatment of Bipolar Disorder; Mania; Migraine Prevention; Seizures; Epilepsy 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 125 mg is not a controlled substance under the Controlled Substances Act (CSA).
Images for THIS END UP RDY 532
Divalproex Sodium Delayed-Release (Sprinkle)
- Imprint
- THIS END UP RDY 532
- Strength
- 125 mg
- Color
- Blue & White
- 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
- Dr. Reddy’s Laboratories Inc.
- National Drug Code (NDC)
- 55111-0532
- Inactive Ingredients
-
ferrosoferric oxide,
D&C Red No. 28,
FD&C Blue No. 1,
ethylcellulose,
gelatin,
hypromelloses,
magnesium stearate,
raw sugar,
titanium dioxide,
triethyl citrate
Note: Inactive ingredients may vary.
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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
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.