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General MedicationsORALGeneric

ATOMOXETINE HYDROCHLORIDE

ATOMOXETINE HYDROCHLORIDE

Standard Dose
100MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: None (Tentative Approval)
Summary

Approval overview ATOMOXETINE HYDROCHLORIDE is listed in Drugs@FDA under application 079020 (ANDA).

Marketing status: None (Tentative Approval) Active ingredient ATOMOXETINE HYDROCHLORIDE Form and strength CAPSULE; ORAL - 100MG Sponsor SUN PHARMA GLOBAL Submission history Latest submission status date: 2012-05-11 00:00:00.

Structured Monograph

Clinical summary

Approval overview ATOMOXETINE HYDROCHLORIDE is listed in Drugs@FDA under application 079020 (ANDA). Marketing status: None (Tentative Approval) Active ingredient ATOMOXETINE HYDROCHLORIDE Form and strength CAPSULE; ORAL - 100MG Sponsor SUN PHARMA GLOBAL Submission history Latest submission status date: 2012-05-11 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: None (Tentative Approval)

Interaction Notes

  • No interaction notes stored yet.