M 177 (Divalproex sodium extended-release 250 mg)

Pill imprint M 177 has been identified as Divalproex sodium extended-release 250 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. 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 subject to the Controlled Substances Act.

See also related documents.

Images for M 177 (Divalproex sodium extended-release 250 mg)

Divalproex sodium extended-release 250 mg M 177
Divalproex sodium extended-release 250 mg M 177  Front
Divalproex sodium extended-release 250 mg M 177  Back
Divalproex sodium extended-release 250 mg M 177
Divalproex sodium extended-release
Imprint:
M 177
Strength:
250 mg
Color:
White
Size:
12.00 mm
Shape:
Round
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:
N - Not a controlled drug
Manufacturer:
Mylan Pharmaceuticals Inc.
National Drug Code (NDC):
00378-0472
Inactive Ingredients:
ammonia
silicon dioxide
dibutyl sebacate
ethylcelluloses
hypromelloses
oleic acid
polydextrose
polyethylene glycol
microcrystalline cellulose
titanium dioxide
triacetin
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
51079-0766 UDL Laboratories Inc

Note: Inactive ingredients may vary.

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