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512 (Divalproex Sodium Delayed Release 250 mg)

Pill with imprint 512 is Brown, Elliptical / Oval and has been identified as Divalproex Sodium Delayed Release 250 mg. It is supplied by Northstar Rx LLC.

Divalproex sodium is used in the treatment of bipolar disorder; epilepsy; mania; migraine prevention; 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 250 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for 512

Divalproex sodium delayed release 250 mg 512

Divalproex Sodium Delayed Release

Imprint:
512
Strength:
250 mg
Color:
Brown
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:
Not a controlled drug
Labeler / Supplier:
Northstar Rx LLC
Inactive Ingredients:
corn starch
povidone k29/32
microcrystalline cellulose
silicon dioxide
methacrylic acid - ethyl acrylate copolymer (1:1) type a
sodium hydroxide
triethyl citrate
magnesium silicate
ferric oxide red
Note: Inactive ingredients may vary.

Other Labelers / Repackagers:

NDC CodeLabeler / Repackager
63739-0553 McKesson Packaging Services

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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