10370-511 : Divalproex Sodium 500 mg 24 Hr Extended Release Tablet


NDC: 10370-511
Labeler: Par Pharmaceutical, Inc.
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium Extended-release
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA078445
Rev. Date: 


Appearance:


Markings: A511
Shapes:  Oval
Colors:  White
Size (mm): 19
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.

A511: (10370-511) Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Par Pharmaceutical, Inc.
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 10370-511-10: 100 TABLET, EXTENDED RELEASE IN 1 BOTTLE (10370‑511‑10)
  • 10370-511-50: 500 TABLET, EXTENDED RELEASE IN 1 BOTTLE (10370‑511‑50)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Hypromelloses
  • Silicon Dioxide
  • Magnesium Stearate
  • Talc
  • Titanium Dioxide
  • Povidones
  • Polyethylene Glycols
  • Ferrosoferric Oxide
  • Ethylcelluloses
  • Hydroxyethyl Cellulose (4000 Mpa.s At 1%)

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.
  • 10370-510 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Par Pharmaceutical, Inc.
  • 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.
  • 0378-0473 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Mylan Pharmaceuticals Inc.
  • 0378-1043 Divalproex Sodium 125 mg Delayed Release Tablet by Mylan Pharmaceutical Inc.
  • 0378-1044 Divalproex Sodium 250 mg Delayed Release Tablet by Mylan Pharmaceutical Inc.
  • 0378-1045 Divalproex Sodium 500 mg Delayed Release Tablet by Mylan Pharmaceutical Inc.
  • 0378-8008 Divalproex Sodium 125 mg Delayed Release Capsule by Mylan Pharmaceuticals Inc.
  • 0603-3441 Divalproex Sodium 125 mg Delayed Release Tablet by Qualitest Pharmaceuticals
  • 0603-3442 Divalproex Sodium 250 mg Delayed Release Tablet by Qualitest Pharmaceuticals
  • 0603-3443 Divalproex Sodium 500 mg Delayed Release Tablet by Qualitest Pharmaceuticals
  • 0615-1393 Divalproex Sodium 125 mg Delayed Release Capsule by Ncs Healthcare of Ky, Inc Dba Vangard Labs
  • More related products ...

NDC QR Code

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NDC 10370-511 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.