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General MedicationsORALGeneric

VENLAFAXINE HYDROCHLORIDE

VENLAFAXINE HYDROCHLORIDE

Standard Dose
75MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: None (Tentative Approval)
Summary

Approval overview VENLAFAXINE HYDROCHLORIDE is listed in Drugs@FDA under application 078057 (ANDA).

Marketing status: None (Tentative Approval) Active ingredient VENLAFAXINE HYDROCHLORIDE Form and strength CAPSULE, EXTENDED RELEASE; ORAL - 75MG Sponsor IMPAX LABS Submission history Latest submission status date: 2007-10-16 00:00:00.

Structured Monograph

Clinical summary

Approval overview VENLAFAXINE HYDROCHLORIDE is listed in Drugs@FDA under application 078057 (ANDA). Marketing status: None (Tentative Approval) Active ingredient VENLAFAXINE HYDROCHLORIDE Form and strength CAPSULE, EXTENDED RELEASE; ORAL - 75MG Sponsor IMPAX LABS Submission history Latest submission status date: 2007-10-16 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: None (Tentative Approval)

Interaction Notes

  • No interaction notes stored yet.