Skip to Content

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; mania; epilepsy; migraine prevention 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.

Labelers / Repackagers

NDC CodeLabeler / Repackager
16714-0512 NorthStar Rx LLC
63739-0553 McKesson Packaging Services

Get help with Imprint Code FAQs.

Related Images for "512"

Further information

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