57962-014 : Imbruvica 140 mg Oral Tablet, Film Coated


NDC57962-014
Labeler: Pharmacyclics LLC
Product Type: Human Prescription Drug
Drug Name:  Imbruvica
Dosage Form: Oral Tablet, Film Coated
Application #: NDA210563
Rev. Date: 


Appearance:


Markings: ibr;140
Shapes:  Round
Colors:  Green
Size (mm): 9
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:

  • 57962-014-28: 1 BLISTER PACK IN 1 CARTON (57962‑014‑28) > 28 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Ibrutinib

Dosage Strength:

  • 140 mg

Pharmaceutical Classes:

  • Kinase Inhibitor [EPC]
  • Protein Kinase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 57962-007 Imbruvica 70 mg/ml Oral Suspension by Pharmacyclics LLC
  • 57962-070 Imbruvica 70 mg Oral Capsule by Pharmacyclics LLC
  • 57962-280 Imbruvica 280 mg Oral Tablet, Film Coated by Pharmacyclics LLC
  • 57962-420 Imbruvica 420 mg Oral Tablet, Film Coated by Pharmacyclics LLC
  • 57962-560 Imbruvica 560 mg Oral Tablet, Film Coated by Pharmacyclics LLC
  • 57962-140 Imbruvica (Ibrutinib 140 mg) by Pharmacyclics, Inc

NDC QR Code

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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.