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General MedicationsORALStandard

RAMELTEON

RAMELTEON

Standard Dose
8MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview RAMELTEON is listed in Drugs@FDA under application 216209 (ANDA).

Review priority: STANDARD Marketing status: Prescription Active ingredient RAMELTEON Form and strength TABLET;ORAL - 8MG Sponsor XIROMED Submission history Latest submission status date: 2022-11-25 00:00:00.

Structured Monograph

Clinical summary

Approval overview RAMELTEON is listed in Drugs@FDA under application 216209 (ANDA). Review priority: STANDARD Marketing status: Prescription Active ingredient RAMELTEON Form and strength TABLET;ORAL - 8MG Sponsor XIROMED Submission history Latest submission status date: 2022-11-25 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: Prescription
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.