70518-4284 : Trintellix 10 mg Oral Tablet, Film Coated


NDC: 70518-4284
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Trintellix
Dosage Form: Oral Tablet, Film Coated
Application #: NDA204447
Rev. Date: 


NDC Package Codes:

  • 70518-4284-0: 30 POUCH IN 1 BOX (70518‑4284‑0) / 1 TABLET, FILM COATED IN 1 POUCH (70518‑4284‑1)

Active Ingredients:

  • Vortioxetine Hydrobromide

Dosage Strength:

  • 10 mg

Related Products:

Based on records with the same trade name.
  • 70518-2642 Trintellix 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 70518-4483 Trintellix 5 mg Oral Tablet, Film Coated by Remedyrepack Inc.
  • 55154-0256 Trintellix 10 mg Oral Tablet, Film Coated by Cardinal Health
  • 55154-0257 Trintellix 20 mg Oral Tablet, Film Coated by Cardinal Health
  • 64764-720 Trintellix 5 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
  • 64764-730 Trintellix 10 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
  • 64764-740 Trintellix 15 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
  • 64764-750 Trintellix 20 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
  • 69189-0732 Trintellix 10 mg Oral Tablet, Film Coated by Avera Mckennan Hospital

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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.