Skip to Content

512 (Divalproex sodium delayed release 250 mg)

Pill imprint 512 has been identified as Divalproex sodium delayed release 250 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 250 mg is not a controlled substance under the Controlled Substance Act (CSA).

Divalproex sodium delayed release 250 mg 512
Discount Card Promo
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
Manufacturer:
Northstar Rx LLC
National Drug Code (NDC):
16714-0512
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
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
63739-0553 McKesson Packaging Services

Note: Inactive ingredients may vary.

More info Print Imprint Search

Disclaimer: Every effort has been made to ensure that the information provided is accurate, up-to-date, and complete, but no guarantee is made to that effect. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 2016 Drugs.com, National Library of Medicine, Truven Health Analytics and Cerner Multum, Inc. All Rights Reserved.

Hide