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General MedicationsTABLETGeneric

RUXOLITINIB

RUXOLITINIB

Standard Dose
15MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: None (Tentative Approval)
Summary

Approval overview RUXOLITINIB is listed in Drugs@FDA under application 220375 (ANDA).

Review priority: STANDARD Marketing status: None (Tentative Approval) Active ingredient RUXOLITINIB Form and strength TABLET - 15MG Sponsor TORRENT PHARMACEUTICALS LTD Submission history Latest submission status date: 2026-03-23 00:00:00.

Structured Monograph

Clinical summary

Approval overview RUXOLITINIB is listed in Drugs@FDA under application 220375 (ANDA). Review priority: STANDARD Marketing status: None (Tentative Approval) Active ingredient RUXOLITINIB Form and strength TABLET - 15MG Sponsor TORRENT PHARMACEUTICALS LTD Submission history Latest submission status date: 2026-03-23 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: None (Tentative Approval)
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.