63020-198 : Alunbrig Kit
| NDC: | 63020-198 |
| Labeler: | Millennium Pharmaceuticals, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Alunbrig |
| Dosage Form: | Kit |
| Application #: | NDA208772 |
| Rev. Date: |
Appearance:
| Markings: | U13 U7 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 15 19 |
| 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:
- 63020-198-30: 1 KIT IN 1 CARTON (63020‑198‑30) * 7 TABLET, FILM COATED IN 1 BOTTLE (63020‑090‑07) * 23 TABLET, FILM COATED IN 1 BOTTLE (63020‑180‑23)
Active Ingredients:
- Brigatinib
Inactive Ingredients:
- Lactose Monohydrate
- Microcrystalline Cellulose
- Sodium Starch Glycolate Type a Potato
- Silicon Dioxide
- Magnesium Stearate
Related Products:
Based on records with the same trade name.- 63020-090 Alunbrig 90 mg Oral Tablet, Film Coated by Millennium Pharmaceuticals, Inc.
- 63020-113 Alunbrig 30 mg Oral Tablet, Film Coated by Millennium Pharmaceuticals, Inc.
- 63020-180 Alunbrig 180 mg Oral Tablet, Film Coated by Millennium Pharmaceuticals, Inc.
- 76189-113 Alunbrig 30 mg Oral Tablet, Coated by Ariad Pharmaceuticals 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.