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FDA Drug Approval, N021529, NEXPLANON
FDA Drug Approval, N021529, NEXPLANON
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NDA: 021529
Company: ORGANON
Drug Name: NEXPLANON
Active Ingredients: ETONOGESTREL
Strength: 68MG/IMPLANT
Dosage Form/Route: IMPLANT;IMPLANTATION
Action Date: 07/17/2006
Marketing Status: Prescription
Submission Classification: Type 3 - New Dosage Form
Company: ORGANON
Drug Name: NEXPLANON
Active Ingredients: ETONOGESTREL
Strength: 68MG/IMPLANT
Dosage Form/Route: IMPLANT;IMPLANTATION
Action Date: 07/17/2006
Marketing Status: Prescription
Submission Classification: Type 3 - New Dosage Form
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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