M945 (Divalproex Sodium Delayed-Release 500 mg)
Pill imprint M945 has been identified as Divalproex sodium delayed-release 500 mg.
Divalproex sodium is used in the treatment of bipolar disorder; migraine prevention; mania; epilepsy; hyperekplexia (and more), and belongs to the drug class fatty acid derivative anticonvulsants. There is positive evidence of human fetal risk during pregnancy. Divalproex sodium 500 mg is not subject to the Controlled Substances Act.
See also related documents.
Images for M945 (Divalproex Sodium Delayed-Release 500 mg)
- 500 mg
- 20.00 mm
- Elliptical / Oval
- Prescription only
- Drug Class:
- Fatty acid derivative anticonvulsants
- Pregnancy Category:
- D - Positive evidence of risk
- CSA Schedule:
- N - Not a controlled drug
- Mylan Pharmaceuticals Inc.
- National Drug Code (NDC):
- Inactive Ingredients:
- ferrosoferric oxide
FD&C Blue No. 2
FD&C Yellow No. 6
methacrylic acid - ethyl acrylate copolymer (1:1) type a
|NDC Code||Manufacturer / Repackager|
|51079-0475||UDL Laboratories Inc|
Note: Inactive ingredients may vary.
More about divalproex sodium
- Divalproex delayed-release tablets
- Divalproex extended-release tablets
- Divalproex sprinkle capsules
- Divalproex sodium
- Divalproex sodium (Advanced Reading)
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