797 Pill - orange oval, 15mm
Pill with imprint 797 is Orange, Oval and has been identified as Divalproex Sodium Delayed-Release 250 mg. It is supplied by Sun Pharmaceuticals.
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 797
Divalproex Sodium Delayed-Release
- Imprint
- 797
- Strength
- 250 mg
- Color
- Orange
- 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
- Sun Pharmaceuticals
- National Drug Code (NDC)
- 62756-0797
- Inactive Ingredients
-
silicon dioxide,
corn starch,
povidone,
hypromelloses,
titanium dioxide,
triacetin,
methacrylic acid - ethyl acrylate copolymer (1:1) type a,
triethyl citrate,
sodium bicarbonate,
sodium lauryl sulfate,
FD&C Yellow No. 6,
ferric oxide yellow,
shellac,
ferrosoferric oxide,
butyl alcohol,
propylene glycol,
ammonia,
magnesium silicate
Note: Inactive ingredients may vary.
Related images for "797"
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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
Related treatment guides
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.