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UL 500 Pill: pink, capsule/oblong, 19mm

The pill with imprint UL 500 (Pink, Capsule/Oblong, 19mm) has been identified as Divalproex Sodium Delayed Release 500 mg and is used for Bipolar Disorder, Mania, Migraine Prevention, Seizures, and Epilepsy. It belongs to the drug class fatty acid derivative anticonvulsants and is not a controlled substance.

Images for UL 500

Divalproex sodium delayed release 500 mg UL 500
Divalproex sodium delayed release 500 mg UL 500 Front
Divalproex sodium delayed release 500 mg UL 500 Back
Divalproex sodium delayed release 500 mg UL 500
Divalproex sodium delayed release 500 mg 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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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.