NDC 70518-2642

Trintellix

Vortioxetine

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

• Product ID: 70518-2642_a69174e9-c333-4741-e053-2995a90ad540
• NDC: 70518-2642
• Product Type: Human Prescription Drug
• Proprietary Name: Trintellix
• Generic Name: Vortioxetine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2020-03-24
• Marketing Category: NDA / NDA
• Application Number: NDA204447
• Labeler Name: REMEDYREPACK INC.
• Substance Name: VORTIOXETINE HYDROBROMIDE
• Active Ingredient Strength: 20 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 70518-2642-0

30 POUCH in 1 BOX (70518-2642-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-2642-1)

• Marketing Start Date: 2020-03-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70518-2642-1 [70518264201]

Trintellix TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA204447
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-03-24

NDC 70518-2642-0 [70518264200]

Trintellix TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA204447
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-03-24

Drug Details

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