Skip to main content
MedicHelpLine
Join Free
Verified Professional Network190+ CountriesHIPAA-Aware Platform
Back to Drug Index
General MedicationsORALGeneric

ATOMOXETINE HYDROCHLORIDE

ATOMOXETINE HYDROCHLORIDE

Standard Dose
10MG
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 - 10MG 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 - 10MG 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.