A514 Pill - yellow oval, 19mm
Pill with imprint A514 is Yellow, Oval and has been identified as Divalproex Sodium Delayed Release 500 mg. It is supplied by Anchen Pharmaceuticals, 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 500 mg is not a controlled substance under the Controlled Substances Act (CSA).
Images for A514
Divalproex Sodium Delayed Release
- Imprint
- A514
- Strength
- 500 mg
- Color
- Yellow
- 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
- Anchen Pharmaceuticals, Inc.
- National Drug Code (NDC)
- 24979-0514
- Inactive Ingredients
-
silicon dioxide,
croscarmellose sodium,
magnesium stearate,
microcrystalline cellulose,
povidone,
magnesium silicate,
titanium dioxide,
triethyl citrate,
FD&C Yellow No. 5,
ferric oxide red,
cellacefate
Note: Inactive ingredients may vary.
Related images for "A514"
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Patient resources
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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
Related treatment guides
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.