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General MedicationsORALGeneric

EVEKEO ODT

AMPHETAMINE SULFATE

Standard Dose
10MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview EVEKEO ODT is listed in Drugs@FDA under application 209905 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient AMPHETAMINE SULFATE Form and strength TABLET, ORALLY DISINTEGRATING;ORAL - 10MG Sponsor AZURITY Submission history Latest submission status date: 2023-10-13 00:00:00.

Structured Monograph

Clinical summary

Approval overview EVEKEO ODT is listed in Drugs@FDA under application 209905 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient AMPHETAMINE SULFATE Form and strength TABLET, ORALLY DISINTEGRATING;ORAL - 10MG Sponsor AZURITY Submission history Latest submission status date: 2023-10-13 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
EVEKEO ODT (AMPHETAMINE SULFATE) | Drug Monograph | MedicHelpline