63020-536 : Iclusig 10 mg Oral Tablet, Film Coated


NDC: 63020-536
Labeler: Millennium Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Iclusig
Dosage Form: Oral Tablet, Film Coated
Application #: NDA203469
Rev. Date: 


NDC Package Codes:

  • 63020-536-30: 30 TABLET, FILM COATED IN 1 BOTTLE (63020‑536‑30)

Active Ingredients:

  • Ponatinib Hydrochloride

Dosage Strength:

  • 10 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 63020-533 Iclusig 30 mg Oral Tablet, Film Coated by Millenium Pharmaceuticals Inc.
  • 63020-534 Iclusig 45 mg Oral Tablet, Film Coated by Millenium Pharmaceuticals Inc.
  • 63020-535 Iclusig 15 mg Oral Tablet, Film Coated by Millenium Pharmaceuticals Inc.
  • 76189-533 Iclusig 30 mg Oral Tablet, Film Coated by Ariad Pharmaceuticals, Inc.
  • 76189-534 Iclusig (As Ponatinib Hydrochloride) 45 mg Oral Tablet by Ariad Pharmaceuticals, Inc.
  • 76189-535 Iclusig (As Ponatinib Hydrochloride) 15 mg Oral Tablet by Ariad Pharmaceuticals, 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.