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General MedicationsORALStandard

LOMAIRA

PHENTERMINE HYDROCHLORIDE

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

Approval overview LOMAIRA is listed in Drugs@FDA under application 203495 (ANDA).

Marketing status: Prescription Active ingredient PHENTERMINE HYDROCHLORIDE Form and strength TABLET;ORAL - 8MG Sponsor AVANTHI INC Submission history Latest submission status date: 2016-09-12 00:00:00.

Structured Monograph

Clinical summary

Approval overview LOMAIRA is listed in Drugs@FDA under application 203495 (ANDA). Marketing status: Prescription Active ingredient PHENTERMINE HYDROCHLORIDE Form and strength TABLET;ORAL - 8MG Sponsor AVANTHI INC Submission history Latest submission status date: 2016-09-12 00:00:00. Submission type: ORIG.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
LOMAIRA (PHENTERMINE HYDROCHLORIDE) | Drug Monograph | MedicHelpline