72028-178 : Wakix 17.8 mg Oral Tablet, Film Coated
| NDC: | 72028-178 |
| Labeler: | Harmony Biosciences, LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Wakix |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA211150 |
| Rev. Date: |
Appearance:
| Markings: | H |
| Shapes: |
Round |
| Colors: |
 White |
| 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:
- 72028-178-03: 1 BOTTLE, PLASTIC IN 1 CARTON (72028‑178‑03) > 30 TABLET, FILM COATED IN 1 BOTTLE, PLASTIC
Active Ingredients:
- Pitolisant Hydrochloride
Dosage Strength:
- 17.8 mg
Inactive Ingredients:
- Silicon Dioxide
- Crospovidone
- Magnesium Stearate
- Microcrystalline Cellulose
- Polyethylene Glycol, Unspecified
- Polyvinyl Alcohol, Unspecified
- Talc
- Titanium Dioxide /
Related Products:
Based on records with the same trade name.- 72028-045 Wakix 4.45 mg Oral Tablet, Film Coated by Harmony Biosciences, LLC
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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.