NDC 64764-730 – Trintellix
Vortioxetine Hydrobromide 10 mg/1 · Tablet, Film Coated · Oral
Product NDC64764-730
Product details
- Brand name
- Trintellix
- Generic name
- Vortioxetine
- Labeler
- Takeda Pharmaceuticals America, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA204447
- Marketed since
- October 2, 2013
- Listing expires
- December 31, 2026
Active ingredients
- Vortioxetine Hydrobromide 10 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 64764-730-07 | 1 BOTTLE in 1 CARTON (64764-730-07) / 7 TABLET, FILM COATED in 1 BOTTLE | Oct 2, 2013 |
| 64764-730-09 | 30 TABLET, FILM COATED in 1 BOTTLE (64764-730-09) | Oct 2, 2013 |
| 64764-730-30 | 30 TABLET, FILM COATED in 1 BOTTLE (64764-730-30) | Oct 2, 2013 |
| 64764-730-77 | 500 TABLET, FILM COATED in 1 BOTTLE (64764-730-77) | Oct 2, 2013 |
| 64764-730-90 | 90 TABLET, FILM COATED in 1 BOTTLE (64764-730-90) | Oct 2, 2013 |
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- 70518-4284 Vortioxetine Hydrobromide 10 mg/1 · Tablet, Film Coated · REMEDYREPACK INC.
- 70518-4483 Vortioxetine Hydrobromide 5 mg/1 · Tablet, Film Coated · REMEDYREPACK INC.
- 64764-720 Vortioxetine Hydrobromide 5 mg/1 · Tablet, Film Coated · Takeda Pharmaceuticals America, Inc.
- 64764-750 Vortioxetine Hydrobromide 20 mg/1 · Tablet, Film Coated · Takeda Pharmaceuticals America, Inc.