797 (Divalproex sodium delayed-release 250 mg)
Pill imprint 797 has been identified as Divalproex sodium delayed-release 250 mg.
Divalproex sodium is used in the treatment of bipolar disorder; mania; migraine prevention; epilepsy; cyclothymic disorder (and more), and belongs to the drug class fatty acid derivative anticonvulsants. There is positive evidence of human fetal risk during pregnancy. Divalproex sodium 250 mg is not subject to the Controlled Substances Act.
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Images for 797 (Divalproex sodium delayed-release 250 mg)
- Imprint:
-
797
- Strength:
- 250 mg
- Color:
- Orange
- Size:
- 15.00 mm
- Shape:
- Elliptical / Oval
- Availability:
- Prescription only
- Drug Class:
- Fatty acid derivative anticonvulsants
- Pregnancy Category:
- D - Positive evidence of risk
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Sun Pharmaceuticals
- National Drug Code (NDC):
- 62756-0797
- Inactive Ingredients:
- silicon dioxide
corn starch
povidone k30
hypromellose
titanium dioxide
triacetin
methacrylic acid - ethyl acrylate copolymer (1:1) type a
magnesium silicate
triethyl citrate
sodium bicarbonate
sodium lauryl sulfate
FD&C Yellow No. 6
ferric oxide yellow
| NDC Code | Manufacturer / Repackager |
|---|---|
| 16590-0809 | Stat RX USA LLC (repackager) |
Note: Inactive ingredients may vary.
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Divalproex sodium delayed-release is associated with the treatment of:
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