52125-048 : Divalproex Sodium 500 mg 24 Hr Extended Release Tablet


NDC52125-048
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium
Dosage Form: Oral Tablet, Film Coated, 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 Remedyrepack 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:

  • 52125-048-02: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK (52125‑048‑02)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Ethylcellulose (10 Mpa.s)
  • Hypromellose 2208 (100 Mpa.s)
  • Silicon Dioxide
  • Magnesium Stearate
  • Talc
  • Titanium Dioxide
  • Povidone K12
  • Polyethylene Glycol 1000000
  • Ferrosoferric Oxide

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.
  • 49349-072 Divalproex Sodium 500 mg Delayed Release Tablet by Remedyrepack Inc.
  • 49349-095 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-101 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-139 Divalproex Sodium 500 mg Delayed Release Tablet by Remedyrepack Inc.
  • 49349-238 Divalproex Sodium 125 mg Delayed Release Tablet by Remedyrepack Inc.
  • 49349-288 Divalproex Sodium 125 mg Delayed Release Tablet by Remedyrepack Inc.
  • 49349-399 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-405 Divalproex Sodium 500 mg 24 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-411 Divalproex Sodium 250 mg 24 Hr Extended Release Tablet by Remedyrepack Inc.
  • 49349-822 Divalproex Sodium 125 mg Delayed Release Tablet by Remedyrepack Inc.
  • 61786-019 Divalproex Sodium 500 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 61786-069 Divalproex Sodium 250 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.
  • 61786-079 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 61786-104 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 61786-175 Divalproex Sodium 125 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0282 Divalproex Sodium 500 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0312 Divalproex Sodium 250 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • 70518-0374 Divalproex Sodium 125 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0463 Divalproex Sodium 250 mg Oral Tablet, Delayed Release by Remedyrepack Inc.
  • 70518-0613 Divalproex Sodium 500 mg Oral Tablet, Extended Release by Remedyrepack Inc.
  • More related products ...

NDC 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.