L007 (Divalproex Sodium Delayed-Release 500 mg)

Pill with imprint L007 is Purple, Elliptical / Oval and has been identified as Divalproex Sodium Delayed-Release 500 mg. It is supplied by Lupin Pharmaceuticals, Inc.

Divalproex sodium is used in the treatment of bipolar disorder; epilepsy; mania; migraine prevention; 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 500 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for L007

Divalproex Sodium Delayed-Release

Imprint:

L007

Strength:

500 mg

Color:

Purple

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:

Lupin Pharmaceuticals, Inc

Inactive Ingredients:

microcrystalline cellulose
D&C Red No. 30
FD&C Blue No. 2
ferric oxide yellow
ferrosoferric oxide
hydroxypropyl cellulose
low substituted hydroxypropyl cellulose
hypromellose phthalate (24% phthalate, 55 cst)
hypromelloses
magnesium stearate
propylene glycol
shellac
silicon dioxide
pregelatinized corn starch
magnesium silicate
titanium dioxide
triethyl citrate
Note: Inactive ingredients may vary.

Other Labelers / Repackagers:

NDC Code	Labeler / Repackager
68084-0315	Amerisource Health Services
54868-6072	Physicians Total Care Inc. (repackager)

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Further information

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