72579-011 : Brukinsa 80 mg Oral Capsule, Gelatin Coated
| NDC: | 72579-011 |
| Labeler: | Beigene USA, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Brukinsa |
| Dosage Form: | Oral Capsule, Gelatin Coated |
| Application #: | NDA213217 |
| Rev. Date: |
Appearance:
| Markings: | Zanu;80 |
| Shapes: |
Capsule |
| Colors: |
 White |
| Size (mm): | 22 |
| 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:
- 72579-011-01: 60 CAPSULE, GELATIN COATED IN 1 BOTTLE, PLASTIC (72579‑011‑01)
- 72579-011-02: 120 CAPSULE, GELATIN COATED IN 1 BOTTLE, PLASTIC (72579‑011‑02)
Active Ingredients:
- Zanubrutinib
Dosage Strength:
- 80 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Magnesium Stearate
- Microcrystalline Cellulose
- Sodium Lauryl Sulfate
- Gelatin, Unspecified
- Titanium Dioxide /
Pharmaceutical Classes:
- Bruton's Tyrosine Kinase Inhibitors [MoA]
- Kinase Inhibitor [EPC]
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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.