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FDA Drug Approval, N071196, TRAZODONE HYDROCHLORIDE
FDA Drug Approval, N071196, TRAZODONE HYDROCHLORIDE
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NDA: 071196
Company: APOTEX INC
Drug Name: TRAZODONE HYDROCHLORIDE
Active Ingredients: TRAZODONE HYDROCHLORIDE
Strength: 300MG
Dosage Form/Route: TABLET;ORAL
Action Date: 03/25/1987
Marketing Status: Prescription
Submission Classification:
Company: APOTEX INC
Drug Name: TRAZODONE HYDROCHLORIDE
Active Ingredients: TRAZODONE HYDROCHLORIDE
Strength: 300MG
Dosage Form/Route: TABLET;ORAL
Action Date: 03/25/1987
Marketing Status: Prescription
Submission Classification:
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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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