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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Other brands
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.