UL 125 Pill - orange capsule/oblong, 12mm
Pill with imprint UL 125 is Orange, Capsule/Oblong and has been identified as Divalproex Sodium Delayed Release 125 mg. It is supplied by Unichem Pharmaceuticals (USA), Inc.
Divalproex sodium is used in the treatment of Bipolar Disorder; Mania; Migraine Prevention; Epilepsy; Seizures 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 125 mg is not a controlled substance under the Controlled Substances Act (CSA).
Images for UL 125
Divalproex Sodium Delayed Release
- Imprint
- UL 125
- Strength
- 125 mg
- Color
- Orange
- Size
- 12.00 mm
- Shape
- Capsule/Oblong
- 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
- Labeler / Supplier
- Unichem Pharmaceuticals (USA), Inc.
- National Drug Code (NDC)
- 29300-0138
- Inactive Ingredients
-
alcohol,
butyl alcohol,
microcrystalline cellulose,
FD&C Yellow No. 6,
ferric oxide yellow,
ferrosoferric oxide,
hypromellose 2910 (6 mPa.s),
isopropyl alcohol,
lactose monohydrate,
methacrylic acid - ethyl acrylate copolymer (1:1) type a,
polyethylene glycol 3000,
propylene glycol,
shellac,
silicon dioxide,
sodium bicarbonate,
sodium lauryl sulfate,
corn starch,
magnesium silicate,
titanium dioxide,
triacetin,
triethyl citrate,
vanillin
Note: Inactive ingredients may vary.
Related images for "UL 125"
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Other brands
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
