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L007 Pill - purple oval, 19mm

Pill with imprint L007 is Purple, 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; mania; epilepsy; migraine prevention 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 500 mg L007

Divalproex Sodium Delayed-Release

500 mg
19.00 mm
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
D&C Red No. 30, FD&C Blue No. 2, ferric oxide yellow, hypromelloses, silicon dioxide, triethyl citrate, microcrystalline cellulose, hypromellose phthalate, low substituted hydroxypropyl cellulose, shellac, magnesium silicate, hydroxypropyl cellulose, magnesium stearate, propylene glycol, titanium dioxide, ferrosoferric oxide, corn starch

Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code Labeler / Repackager
68180-0267 Lupin Pharmaceuticals, Inc.
68084-0315 (Discontinued) Amerisource Health Services
54868-6072 Physicians Total Care Inc. (repackager)

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.