APO 047 250 (Divalproex sodium delayed-release 250 mg)

Pill imprint APO 047 250 has been identified as Divalproex sodium delayed-release 250 mg.

Divalproex sodium is used in the treatment of bipolar disorder; migraine prevention; mania; epilepsy; hyperekplexia (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 250 mg is not subject to the Controlled Substances Act.

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Images for APO 047 250 (Divalproex sodium delayed-release 250 mg)

Divalproex sodium delayed-release 250 mg APO 047 250
Divalproex sodium delayed-release
Imprint:
APO 047
250
Strength:
250 mg
Color:
White
Size:
15.00 mm
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:
N - Not a controlled drug
Manufacturer:
Apotex Corp.
National Drug Code (NDC):
60505-3066
Inactive Ingredients:
hypromellose
methacrylic acid - ethyl acrylate copolymer (1:1) type a
microcrystalline cellulose
polyethylene glycol
magnesium silicate
titanium dioxide
triethyl citrate
hydroxypropyl cellulose

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