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FDA Drug Approval, A090694, DULOXETINE HYDROCHLORIDE
FDA Drug Approval, A090694, DULOXETINE HYDROCHLORIDE
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ANDA: 090694
Company: LUPIN LTD
Drug Name: DULOXETINE HYDROCHLORIDE
Active Ingredients: DULOXETINE HYDROCHLORIDE
Strength: EQ 60MG BASE
Dosage Form/Route: CAPSULE, DELAYED REL PELLETS;ORAL
Action Date: 12/11/2013
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
Company: LUPIN LTD
Drug Name: DULOXETINE HYDROCHLORIDE
Active Ingredients: DULOXETINE HYDROCHLORIDE
Strength: EQ 60MG BASE
Dosage Form/Route: CAPSULE, DELAYED REL PELLETS;ORAL
Action Date: 12/11/2013
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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