UL 500 Pill - pink capsule/oblong, 19mm
Pill with imprint UL 500 is Pink, Capsule/Oblong and has been identified as Divalproex Sodium Delayed Release 500 mg. It is supplied by Unichem Pharmaceuticals (USA), Inc.
Divalproex sodium is used in the treatment of Bipolar Disorder; Mania; Migraine Prevention; Seizures; Epilepsy 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 Substances Act (CSA).
Images for UL 500
Divalproex Sodium Delayed Release
- Imprint
- UL 500
- Strength
- 500 mg
- Color
- Pink
- Size
- 19.00 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)
- 29300-0140
- Inactive Ingredients
-
alcohol,
butyl alcohol,
microcrystalline cellulose,
FD&C Red No. 40,
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.
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