M 473 (Divalproex sodium extended-release 500 mg)

Pill imprint M 473 has been identified as Divalproex sodium extended-release 500 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 500 mg is not a controlled substance under the Controlled Substance Act (CSA).

Divalproex sodium extended-release

Imprint:

M 473

Strength:

500 mg

Color:

White

Size:

21.00 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

Manufacturer:

Mylan Pharmaceuticals Inc.

National Drug Code (NDC):

00378-0473

Inactive Ingredients:

ammonia
silicon dioxide
dibutyl sebacate
ethylcelluloses
hypromelloses
oleic acid
polydextrose
polyethylene glycol
microcrystalline cellulose
titanium dioxide
triacetin

Other Manufacturers / Repackagers:

NDC Code	Manufacturer / Repackager
51079-0767	UDL Laboratories Inc

Note: Inactive ingredients may vary.

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