512 Pill - brown oval, 15mm
Pill with imprint 512 is Brown, 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; Migraine Prevention; Seizures; Epilepsy 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
- Imprint
- 512
- Strength
- 250 mg
- Color
- Brown
- Size
- 15.00 mm
- Shape
- 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 k30,
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 Code | Labeler / Repackager |
|---|---|
| 16714-0512 (Discontinued) | NorthStar Rx LLC |
| 63739-0553 (Discontinued) | McKesson Packaging Services |
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Professional resources
- Divalproex Capsules prescribing information
- Divalproex Delayed Release (FDA)
- Divalproex Delayed Release Tablets (FDA)
- Divalproex Extended Release (FDA)
- Divalproex Sprinkle (FDA)
Other brands
Depakote, Depakote ER, Depakote Sprinkles
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.