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Divalproex Sodium 125 mg Delayed Release Oral Tablet
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Divalproex Sodium 125 mg Delayed Release Oral Tablet

Pill Finder Wizard
Overview Divalproex Sodium 125 mg Delayed Release Oral Tablet is a oval shaped, orange, delayed release tablet that is approximately 12 mm in size. It has one score and can be broken into two pieces.

It is imprinted with "UL" and "125" and is supplied by Remedyrepack Inc.
Drug Name Divalproex Sodium
Dosage Form Delayed Release Tablet
Imprint(s) UL, 125
Pill Size 12 mm
DEA Schedule (Potential for Drug Abuse)
Drug Ingredients
Active Ingredient(s) Divalproex Sodium
Inactive Ingredient(s) Alcohol, Butyl Alcohol, Cellulose, Microcrystalline, FD&C Yellow No. 6, Ferric Oxide Yellow, Ferrosoferric Oxide, Hypromellose 2910, Isopropyl Alcohol, Lactose Monohydrate, Methacrylic Acid - Ethyl Acrylate Copolymer Type A, Polyethylene Glycol 3000, Povidone K29/32, Propylene Glycol, Shellac, Silicon Dioxide, Sodium Bicarbonate, Sodium Lauryl Sulfate, Starch, Pregelatinized Corn, Talc, Titanium Dioxide, Triacetin, Triethyl Citrate, Vanillin
Drug Codes
RxNorm Concept Unique Identifier 1,099,625
National Drug Code 617860175
Marketing Category ANDA
Supplier Remedyrepack Inc.
References The data for Divalproex Sodium 125 mg Delayed Release Oral Tablet was updated by the U.S National Library of Medicine on January 18, 2018.

  • U.S. National Library of Medicine. Accessed June 8, 2019.
  • Drug Scheduling. United States Drug Enforcement Administration. Accessed June 8, 2019.
  • Structured Product Labeling Resources. U.S. Food & Drug Administration. March 27, 2018. Accessed June 8, 2019.
  • HL7 Reference Information Model. HL7 Interational. Accessed June 8, 2019.