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General MedicationsORALStandard

MESALAMINE

MESALAMINE

Standard Dose
800MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview MESALAMINE is listed in Drugs@FDA under application 215067 (ANDA).

Review priority: STANDARD Marketing status: Prescription Active ingredient MESALAMINE Form and strength TABLET, DELAYED RELEASE;ORAL - 800MG Sponsor AMNEAL Submission history Latest submission status date: 2025-02-18 00:00:00.

Structured Monograph

Clinical summary

Approval overview MESALAMINE is listed in Drugs@FDA under application 215067 (ANDA). Review priority: STANDARD Marketing status: Prescription Active ingredient MESALAMINE Form and strength TABLET, DELAYED RELEASE;ORAL - 800MG Sponsor AMNEAL Submission history Latest submission status date: 2025-02-18 00:00:00. Submission type: ORIG.

Monitoring

  • Marketing status: Prescription
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.