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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; 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

Imprint
L007
Strength
500 mg
Color
Purple
Size
19.00 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
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 (24% phthalate, 55 cst), low substituted hydroxypropyl cellulose, shellac, magnesium silicate, hydroxypropyl cellulose (type h), magnesium stearate, propylene glycol, titanium dioxide, ferrosoferric oxide, pregelatinized corn starch

Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC CodeLabeler / Repackager
68180-0267 Lupin Pharmaceuticals, Inc.
68084-0315 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.