A514 (Divalproex Sodium Delayed Release 500 mg)

Pill imprint A514 has been identified as Divalproex sodium delayed release 500 mg.

Divalproex sodium is used in the treatment of bipolar disorder; mania; migraine prevention; epilepsy; borderline personality disorder (and more), 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 Substance Act (CSA).

Divalproex sodium delayed release

Imprint:

A514

Strength:

500 mg

Color:

Yellow

Shape:

Elliptical / 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

Manufacturer:

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

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