DailyMed - Search Results for vortioxetine hydrobromide

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TRINTELLIX (vortioxetine) tablet, film coated

NDC Code(s):

64764-720-07, 64764-720-09, 64764-720-30, 64764-720-77, view more

64764-720-90, 64764-730-07, 64764-730-09, 64764-730-30, 64764-730-77, 64764-730-90, 64764-750-07, 64764-750-09, 64764-750-30, 64764-750-77, 64764-750-90

Packager: Takeda Pharmaceuticals America, Inc.

TRINTELLIX (vortioxetine) tablet, film coated

NDC Code(s):

55154-0256-8, 55154-0257-8

Packager: Cardinal Health 107, LLC
This is a repackaged label.
Source NDC Code(s): 64764-730, 64764-750

TRINTELLIX (vortioxetine) tablet, film coated

NDC Code(s):

70518-4284-0, 70518-4284-1

Packager: REMEDYREPACK INC.
This is a repackaged label.
Source NDC Code(s): 64764-730

TRINTELLIX (vortioxetine) tablet, film coated

NDC Code(s):

70518-2642-0, 70518-2642-1

Packager: REMEDYREPACK INC.
This is a repackaged label.
Source NDC Code(s): 64764-750

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SEARCH RESULTS for: vortioxetine hydrobromide (4 results)

TRINTELLIX (vortioxetine) tablet, film coated

TRINTELLIX (vortioxetine) tablet, film coated

TRINTELLIX (vortioxetine) tablet, film coated

TRINTELLIX (vortioxetine) tablet, film coated

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