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General MedicationsINTRAMUSCULARGeneric

PALIPERIDONE PALMITATE

PALIPERIDONE PALMITATE

Standard Dose
39MG/0.25ML
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: None (Tentative Approval)
Summary

Approval overview PALIPERIDONE PALMITATE is listed in Drugs@FDA under application 211995 (ANDA).

Review priority: STANDARD Marketing status: None (Tentative Approval) Active ingredient PALIPERIDONE PALMITATE Form and strength SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR - 39MG/0.25ML Sponsor TOLMAR Submission history Latest submission status date: 2023-06-30 00:00:00.

Structured Monograph

Clinical summary

Approval overview PALIPERIDONE PALMITATE is listed in Drugs@FDA under application 211995 (ANDA). Review priority: STANDARD Marketing status: None (Tentative Approval) Active ingredient PALIPERIDONE PALMITATE Form and strength SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR - 39MG/0.25ML Sponsor TOLMAR Submission history Latest submission status date: 2023-06-30 00:00:00. Submission type: ORIG.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.