68462-714 : Rufinamide 400 mg Oral Tablet, Film Coated


NDC68462-714
Labeler: Glenmark Pharmaceuticals Inc., USA
Product Type: Human Prescription Drug
Drug Name:  Rufinamide
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA205075
Rev. Date: 


NDC Package Codes:

  • 68462-714-05: 500 TABLET, FILM COATED IN 1 BOTTLE (68462‑714‑05)
  • 68462-714-08: 120 TABLET, FILM COATED IN 1 BOTTLE (68462‑714‑08)

Active Ingredients:

  • Rufinamide

Dosage Strength:

  • 400 mg

Related Products:

Based on records with the same trade name.
  • 68462-713 Rufinamide 200 mg Oral Tablet, Film Coated by Glenmark Pharmaceuticals Inc., USA
  • 0054-0425 Rufinamide 200 mg Oral Tablet, Film Coated by Hikma Pharmaceuticals USA Inc.
  • 0054-0426 Rufinamide 400 mg Oral Tablet, Film Coated by Hikma Pharmaceuticals USA Inc.
  • 0054-0528 Rufinamide 40 mg/ml Oral Suspension by Hikma Pharmaceuticals USA Inc.
  • 0378-2330 Rufinamide 200 mg Oral Tablet, Film Coated by Mylan Pharmaceuticals Inc.
  • 0378-2331 Rufinamide 400 mg Oral Tablet, Film Coated by Mylan Pharmaceuticals Inc.
  • 31722-598 Rufinamide 200 mg Oral Tablet, Film Coated by Camber Pharmaceuticals, Inc.
  • 31722-599 Rufinamide 400 mg Oral Tablet, Film Coated by Camber Pharmaceuticals, Inc.
  • 67877-673 Rufinamide 40 mg/ml Oral Suspension by Ascend Laboratories, LLC
  • 69452-223 Rufinamide 40 mg/ml Oral Suspension by Bionpharma Inc.

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