M 944 (Divalproex Sodium Delayed-Release 250 mg)

Pill imprint M 944 has been identified as Divalproex sodium delayed-release 250 mg.

Divalproex sodium is used in the treatment of bipolar disorder; migraine prevention; mania; hyperekplexia; epilepsy (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.

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Divalproex sodium delayed-release 250 mg M 944
Divalproex sodium delayed-release 250 mg M 944
Divalproex sodium delayed-release
Imprint:
M 944
Strength:
250 mg
Color:
Blue
Size:
11.00 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):
00378-1044
Inactive Ingredients:
ferrosoferric oxide
silicon dioxide
copovidone
croscarmellose sodium
FD&C Blue No. 2
FD&C Yellow No. 6
hypromelloses
lactose monohydrate
methacrylic acid - ethyl acrylate copolymer (1:1) type a
microcrystalline cellulose
polydextrose
polyethylene glycol
polysorbate 80
polyvinyl alcohol
propylene glycol
sodium hydroxide
magnesium silicate
titanium dioxide
triacetin
triethyl citrate
Other Manufacturers / Repackagers:
NDC CodeManufacturer / Repackager
51079-0474 UDL Laboratories Inc

Note: Inactive ingredients may vary.

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