797 (Divalproex Sodium Delayed-Release 250 mg)

Pill with imprint 797 is Orange, Elliptical / 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; 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:

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:

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.

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