0228-2144 : Divalproex Sodium 250 mg Delayed Release Tablet


NDC0228-2144
Labeler: Orchid Healthcare (A Division of Orchid Chemicals and Pharmaceuticals Ltd.)
Drug Name: Divalproex Sodium Delayed-release
Rev. Date: 


Appearance:


Shapes:  Oval
Colors:  Brown
Size (mm): 15
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
  • Ferric Oxide
  • Opacode Black

Related Products:

Based on records with the same trade name.
  • 0228-2142 Divalproex Sodium 125 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 0228-2144 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.