63020-535 : Iclusig 15 mg Oral Tablet, Film Coated
| NDC: | 63020-535 |
| Labeler: | Millenium Pharmaceuticals Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Iclusig |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA203469 |
| Rev. Date: |
Appearance:
| Markings: | A5 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 6 |
| 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:
- 63020-535-30: 30 TABLET, FILM COATED IN 1 BOTTLE (63020‑535‑30)
- 63020-535-60: 60 TABLET, FILM COATED IN 1 BOTTLE (63020‑535‑60)
Active Ingredients:
- Ponatinib Hydrochloride
Dosage Strength:
- 15 mg
Inactive Ingredients:
- Lactose Monohydrate
- Microcrystalline Cellulose
- Sodium Starch Glycolate Type B Potato
- Silicon Dioxide
- Magnesium Stearate
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.
- 63020-536 Iclusig 10 mg Oral Tablet, Film Coated by Millennium 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.
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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.