NDC 64764-750

Trintellix

Vortioxetine

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

• Product ID: 64764-750_589ba889-a7a8-4904-8912-43fca05c9a6a
• NDC: 64764-750
• 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: Takeda Pharmaceuticals America, Inc.
• Substance Name: VORTIOXETINE HYDROBROMIDE
• Active Ingredient Strength: 20 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 64764-750-07

1 BOTTLE in 1 CARTON (64764-750-07) > 7 TABLET, FILM COATED in 1 BOTTLE

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

NDC SPL Data Element Entries

NDC 64764-750-90 [64764075090]

Trintellix TABLET, FILM COATED

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

NDC 64764-750-09 [64764075009]

Trintellix TABLET, FILM COATED

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

NDC 64764-750-77 [64764075077]

Trintellix TABLET, FILM COATED

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

NDC 64764-750-07 [64764075007]

Trintellix TABLET, FILM COATED

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

NDC 64764-750-30 [64764075030]

Trintellix TABLET, FILM COATED

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

Drug Details

Active Ingredients

Ingredient	Strength
VORTIOXETINE HYDROBROMIDE	20 mg/1

OpenFDA Data

• SPL SET ID: 1a5b68e2-14d0-419d-9ec6-1ca97145e838
• Manufacturer:
  • Takeda Pharmaceuticals America, Inc.
• UNII:
  • TKS641KOAY
• RxNorm Concept Unique ID - RxCUI:
  • 1790886
  • 1790890
  • 1790892
  • 1439808
  • 1439810
  • 1439812
• UPC Code:
  • 0364764730307
  • 0364764750305
  • 0364764720308

Medicade Reported Pricing

64764075030 TRINTELLIX 20 MG TABLET

Pricing Unit: EA | Drug Type:

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