63020-090 : Alunbrig 90 mg Oral Tablet, Film Coated

Labeler: Millennium Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Alunbrig
Dosage Form: Oral Tablet, Film Coated
Application #: NDA208772
Rev. Date: 


Markings: U7
Shapes:  Oval
Colors:  White
Size (mm): 15
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:

  • 63020-090-07: 7 TABLET, FILM COATED IN 1 BOTTLE (63020‑090‑07)
  • 63020-090-30: 30 TABLET, FILM COATED IN 1 BOTTLE (63020‑090‑30)

Active Ingredients:

  • Brigatinib

Dosage Strength:

  • 90 mg

Inactive Ingredients:

  • Lactose Monohydrate
  • Microcrystalline Cellulose
  • Sodium Starch Glycolate Type a Potato
  • Silicon Dioxide
  • Magnesium Stearate

Pharmaceutical Classes:

  • Cytochrome P450 3A Inducers [MoA]
  • Kinase Inhibitor [EPC]
  • Tyrosine Kinase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 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.
  • 63020-198 Alunbrig Kit 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.