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General MedicationsBUCCALGeneric

ONSOLIS

FENTANYL CITRATE

Standard Dose
EQ 0.4MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: N/A Marketing status: Discontinued
Summary

Approval overview ONSOLIS is listed in Drugs@FDA under application 022266 (NDA).

Review priority: N/A Marketing status: Discontinued Active ingredient FENTANYL CITRATE Form and strength FILM;BUCCAL - EQ 0.4MG BASE Sponsor ADALVO Submission history Latest submission status date: 2022-08-17 00:00:00.

Structured Monograph

Clinical summary

Approval overview ONSOLIS is listed in Drugs@FDA under application 022266 (NDA). Review priority: N/A Marketing status: Discontinued Active ingredient FENTANYL CITRATE Form and strength FILM;BUCCAL - EQ 0.4MG BASE Sponsor ADALVO Submission history Latest submission status date: 2022-08-17 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: N/A

Interaction Notes

  • No interaction notes stored yet.