0228-2142 : Divalproex Sodium 125 mg Delayed Release Tablet


NDC0228-2142
Labeler: Orchid Healthcare (A Division of Orchid Chemicals and Pharmaceuticals Ltd.)
Drug Name: Divalproex Sodium Delayed-release
Rev. Date: 


Appearance:


Shapes:  Oval
Colors:  White
Size (mm): 12
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

Active Ingredients:

  • Valproic Acid

Inactive Ingredients:

  • Pregelatinized Starch
  • Povidone
  • Microcrystalline Cellulose
  • Silicon Dioxide
  • Opadry Clear
  • Methacrylic Acid Co-polymer
  • Sodium Hydroxide
  • Simethicone Emulsion
  • Triethyl Citrate
  • Talc
  • Vanilla Flavor
  • Opacode Black

Related Products:

Based on records with the same trade name.
  • 0228-2144 Divalproex Sodium 250 mg Delayed Release Tablet by Orchid Healthcare (A Division of Orchid Chemicals and Pharmaceuticals Ltd.)
  • 0228-2145 Divalproex Sodium 500 mg Delayed Release Tablet by Orchid Healthcare (A Division of Orchid Chemicals and Pharmaceuticals Ltd.)
  • 49349-196 Divalproex Sodium 500 mg Delayed Release Tablet by Remedyrepack Inc.
  • 49349-197 Divalproex Sodium 250 mg Delayed Release Tablet by Remedyrepack Inc.
  • 53808-0681 Divalproex Sodium 500 mg Oral Tablet, Film Coated by State of Florida Doh Central Pharmacy

NDC QR Code

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NDC 0228-2142 QR Code

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