52125-134 : Divalproex Sodium 250 mg Delayed Release Tablet


NDC52125-134
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodiumdelayed-release Delayed-release
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA090210
Rev. Date: 


Appearance:


Markings: 2706;V
Shapes:  Oval
Colors:  Orange
Size (mm): 14
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.

2706 V: (0603-3442) Divalproex Sodium 250 mg Delayed 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:

  • 52125-134-02: 30 TABLET, FILM COATED IN 1 BLISTER PACK (52125‑134‑02)

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Starch, Corn
  • Hypromelloses
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Povidone K12
  • Silicon Dioxide
  • Sodium Bicarbonate
  • Sodium Lauryl Sulfate
  • Talc
  • Titanium Dioxide
  • Triacetin
  • Triethyl Citrate
  • Fd&c Red No. 40
  • Fd&c Yellow No. 6
  • Ferric Oxide Yellow
  • D&c Red No. 27
  • Fd&c Blue No. 2

Pharmaceutical Classes:

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

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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.