L005
Pill imprint L005 has been identified as Divalproex sodium delayed-release 125 mg.
Divalproex sodium is used in the treatment of bipolar disorder; migraine prevention; mania; epilepsy; hyperekplexia and belongs to the drug class fatty acid derivative anticonvulsants. There is positive evidence of human fetal risk during pregnancy.
Divalproex sodium 125 mg is not subject to the Controlled Substances Act.
See also related documents.
Divalproex sodium delayed-release Images
- Imprint:
-
L005
- Strength:
- 125 mg
- Color:
- Purple
- Shape:
- Elliptical / Oval
- Availability:
- Prescription only
- Drug Class:
- Fatty acid derivative anticonvulsants
- Pregnancy Category:
- D - Positive evidence of risk
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Lupin Pharmaceuticals, Inc
- National Drug Code (NDC):
- 68180-0265
More Divalproex Sodium Delayed-Release resources
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- Alti-Valproic (Micromedex) - Includes Dosage Information
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- Depakote Pellets (FDA)
- Divalproex (FDA)
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- Divalproex Delayed Release (FDA)
- Divalproex Extended Release (FDA)
- Divalproex Sprinkle (FDA)


