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L006 (Divalproex sodium delayed-release 250 mg)

Pill imprint L006 has been identified as Divalproex sodium delayed-release 250 mg.

Divalproex sodium is used in the treatment of bipolar disorder; mania; migraine prevention; epilepsy; 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 250 mg is not a controlled substance under the Controlled Substance Act (CSA).

Divalproex sodium delayed-release 250 mg L006
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Divalproex sodium delayed-release
Imprint:
L006
Strength:
250 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
Manufacturer:
Lupin Pharmaceuticals, Inc
National Drug Code (NDC):
68180-0266
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
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
68084-0314 Amerisource Health Services

Note: Inactive ingredients may vary.

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