NDC 55154-0257

Trintellix

Vortioxetine

Trintellix is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Cardinal Health. The primary component is Vortioxetine Hydrobromide.

• Product ID: 55154-0257_0cc35239-79cc-4787-8b43-673e10e3b06e
• NDC: 55154-0257
• Product Type: Human Prescription Drug
• Proprietary Name: Trintellix
• Generic Name: Vortioxetine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2013-10-02
• Marketing Category: NDA / NDA
• Application Number: NDA204447
• Labeler Name: Cardinal Health
• Substance Name: VORTIOXETINE HYDROBROMIDE
• Active Ingredient Strength: 20 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 55154-0257-8

2430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0257-8)

• Marketing Start Date: 2013-10-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55154-0257-8 [55154025708]

Trintellix TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA204447
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2013-10-02

Drug Details

Active Ingredients

Ingredient	Strength
VORTIOXETINE HYDROBROMIDE	20 mg/1

OpenFDA Data

• SPL SET ID: cb1e9df4-dd74-4073-9d78-bb55593dd000
• Manufacturer:
  • Cardinal Health
• UNII:
  • TKS641KOAY
• RxNorm Concept Unique ID - RxCUI:
  • 1439810
  • 1790886
  • 1790890
  • 1439808
• UPC Code:
  • 0355154025783
  • 0355154025684

NDC Crossover Matching brand name "Trintellix" or generic name "Vortioxetine"

NDC	Brand Name	Generic Name
55154-0256	Trintellix	vortioxetine
55154-0257	Trintellix	vortioxetine
64764-720	Trintellix	vortioxetine
64764-730	Trintellix	vortioxetine
64764-750	Trintellix	vortioxetine
70518-2642	Trintellix	Trintellix
64764-550	Brintellix	vortioxetine
64764-560	Brintellix	vortioxetine
64764-570	Brintellix	vortioxetine
64764-580	Brintellix	vortioxetine