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FDA Drug Approval, N019926, HEXALEN
FDA Drug Approval, N019926, HEXALEN
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NDA: 019926
Company: EISAI INC
Drug Name: HEXALEN
Active Ingredients: ALTRETAMINE
Strength: 50MG
Dosage Form/Route: CAPSULE;ORAL
Action Date: 12/26/1990
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
Company: EISAI INC
Drug Name: HEXALEN
Active Ingredients: ALTRETAMINE
Strength: 50MG
Dosage Form/Route: CAPSULE;ORAL
Action Date: 12/26/1990
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
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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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