71610-031 : Divalproex Sodium 250 mg Oral Tablet, Delayed Release


NDC: 71610-031
Labeler: Aphena Pharma Solutions - Tennessee, LLC
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA078182
Rev. Date: 


Appearance:


Markings: U;S;250
Shapes:  Oval
Colors:  Pink
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.

NDC Package Codes:

  • 71610-031-60: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (71610‑031‑60)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Povidone, Unspecified
  • Starch, Corn
  • Silicon Dioxide
  • Sodium Bicarbonate
  • Sodium Lauryl Sulfate
  • Talc
  • Triethyl Citrate
  • Titanium Dioxide
  • Vanillin
  • Fd&c Yellow No. 6
  • Ferric Oxide Red /

Pharmaceutical Classes:

  • Anti-epileptic Agent [EPC]
  • Decreased Central Nervous System Disorganized Electrical Activity [PE]
  • Mood Stabilizer [EPC]

Related Products:

Based on records with the same trade name.
  • 71610-030 Divalproex Sodium 250 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-032 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-157 Divalproex Sodium 250 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-201 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-205 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-249 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-289 Divalproex Sodium 250 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-311 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 71610-707 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 43353-547 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Aphena Pharma Solutions - Tennessee, LLC
  • 0074-0805 Divalproex Sodium by Abbvie Inc.
  • 0093-7439 Divalproex Sodium 125 mg Delayed Release Tablet by Teva Pharmaceuticals USA Inc
  • 0093-7440 Divalproex Sodium (Valproic Acid 250 mg) by Teva Pharmaceuticals USA Inc
  • 0093-7441 Divalproex Sodium 500 mg Delayed Release Tablet by Teva Pharmaceuticals USA Inc
  • 0115-6911 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
  • 0115-6922 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Global Pharmaceuticals, Division of Impax Laboratories Inc.
  • 0245-0180 Divalproex Sodium 125 mg Delayed Release Tablet by Upsher-smith Laboratories, Inc.
  • 0245-0181 Divalproex Sodium 250 mg Delayed Release Tablet by Upsher-smith Laboratories, Inc.
  • 0245-0182 Divalproex Sodium 500 mg Delayed Release Tablet by Upsher-smith Laboratories, Inc.
  • 0378-0472 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
  • More related products ...

NDC QR Code

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NDC 71610-031 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.