75929-098 : Banzel 400 mg Oral Tablet, Film Coated


NDC: 75929-098
Labeler: Pharma Packaging Solutions, LLC Dba Tjoapack LLC
Product Type: Human Prescription Drug
Drug Name:  Banzel
Dosage Form: Oral Tablet, Film Coated
Application #: NDA021911
Rev. Date: 


NDC Package Codes:

  • 75929-098-12: 120 TABLET, FILM COATED IN 1 BOTTLE (75929‑098‑12)
  • 75929-098-51: 120 TABLET, FILM COATED IN 1 BOTTLE (75929‑098‑51)

Active Ingredients:

  • Rufinamide

Dosage Strength:

  • 400 mg

Related Products:

Based on records with the same trade name.
  • 62856-582 Banzel 200 mg Oral Tablet by Eisai Inc.
  • 62856-583 Banzel 400 mg Oral Tablet by Eisai Inc.
  • 62856-584 Banzel 40 mg/ml Oral Suspension by Eisai Inc.
  • 68180-797 Banzel 40 mg/ml Oral Suspension by Lupin Pharmaceuticals, Inc.

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Related Discussions:

Anyone have experience with banzel?
My son is on banzel(along with 280ml of phenobarbital and1200 of keppra)for seizures. He's non verbal so he can'... 1 reply




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