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; cyclothymic disorder (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.
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Images for M 473 (Divalproex sodium extended-release 500 mg)
- 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
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Mylan Pharmaceuticals Inc.
- National Drug Code (NDC):
- 00378-0473
- Inactive Ingredients:
- ammonia
silicon dioxide
dibutyl sebacate
ethylcellulose
hypromellose
oleic acid
polydextrose
polyethylene glycol
microcrystalline cellulose
titanium dioxide
triacetin
| NDC Code | Manufacturer / Repackager |
|---|---|
| 51079-0767 | UDL Laboratories Inc |
Note: Inactive ingredients may vary.
More resources
Divalproex sodium extended-release is associated with the treatment of:
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