55154-6637 : Divalproex Sodium 250 mg/1 Oral Tablet, Delayed Release


NDC55154-6637
Labeler: Cardinal Health
Product Type: Human Prescription Drug
Drug Name:  Divalproex Sodium Dr
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA078790
Rev. Date: 


Appearance:


Markings: L006
Shapes:  Oval
Colors:  Purple
Size (mm): 15
Segments: * 2

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces.

NDC Package Codes:

  • 55154-6637-0: 10 BLISTER PACK IN 1 BAG (55154‑6637‑0) > 1 TABLET, DELAYED RELEASE IN 1 BLISTER PACK

Active Ingredients:

  • Divalproex Sodium

Dosage Strength:

  • 250 mg

Inactive Ingredients:

  • Silicon Dioxide
  • D&c Red No. 30
  • Fd&c Blue No. 2
  • Hydroxypropyl Cellulose (Type H)
  • Hypromelloses
  • Ferrosoferric Oxide
  • Hydroxypropyl Cellulose, Low Substituted
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Propylene Glycol
  • Starch, Corn
  • Shellac
  • Talc
  • Titanium Dioxide
  • Triethyl Citrate

Pharmaceutical Classes:

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

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.