69189-0732 : Trintellix 10 mg Oral Tablet, Film Coated
NDC: | 69189-0732 |
Labeler: | Avera Mckennan Hospital |
Product Type: | Human Prescription Drug |
Drug Name: | Trintellix |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | NDA204447 |
Rev. Date: |
Appearance:
Markings: | 10;TL |
Shapes: |
Tear |
Colors: |
Yellow |
Size (mm): | 8 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
NDC Package Codes:
- 69189-0732-1: 1 TABLET, FILM COATED IN 1 DOSE PACK (69189‑0732‑1)
Active Ingredients:
- Vortioxetine Hydrobromide
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Mannitol
- Microcrystalline Cellulose
- Hydroxypropyl Cellulose (120000 Mw)
- Sodium Starch Glycolate Type a Potato
- Magnesium Stearate
- Hypromellose 2910 (6 Mpa.s)
- Titanium Dioxide
- Polyethylene Glycol 400
- Ferric Oxide Yellow
Related Products:
Based on records with the same trade name.- 55154-0256 Trintellix 10 mg Oral Tablet, Film Coated by Cardinal Health
- 55154-0257 Trintellix 20 mg Oral Tablet, Film Coated by Cardinal Health
- 64764-720 Trintellix 5 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
- 64764-730 Trintellix 10 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
- 64764-740 Trintellix 15 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
- 64764-750 Trintellix 20 mg Oral Tablet, Film Coated by Takeda Pharmaceuticals America, Inc.
- 70518-2642 Trintellix 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.