50881-025 : Jakafi 25 mg Oral Tablet


NDC: 50881-025
Labeler: Incyte Corporation
Product Type: Human Prescription Drug
Drug Name:  Jakafi
Dosage Form: Oral Tablet
Application #: NDA202192
Rev. Date: 


Appearance:


Markings: INCY;25
Shapes:  Oval
Colors:  White
Size (mm): 18
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:

  • 50881-025-60: 60 TABLET IN 1 BOTTLE, PLASTIC (50881‑025‑60)

Active Ingredients:

  • Ruxolitinib

Dosage Strength:

  • 25 mg

Inactive Ingredients:

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

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 50881-005 Jakafi 5 mg Oral Tablet by Incyte Corporation
  • 50881-010 Jakafi 10 mg Oral Tablet by Incyte Corporation
  • 50881-015 Jakafi 15 mg Oral Tablet by Incyte Corporation
  • 50881-020 Jakafi 20 mg Oral Tablet by Incyte Corporation

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 50881-025 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.