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FDA Drug Approval, N017810, PROSTIN E2
FDA Drug Approval, N017810, PROSTIN E2
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NDA: 017810
Company: PFIZER
Drug Name: PROSTIN E2
Active Ingredients: DINOPROSTONE
Strength: 20MG
Dosage Form/Route: SUPPOSITORY;VAGINAL
Action Date: 08/23/1977
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity
Company: PFIZER
Drug Name: PROSTIN E2
Active Ingredients: DINOPROSTONE
Strength: 20MG
Dosage Form/Route: SUPPOSITORY;VAGINAL
Action Date: 08/23/1977
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 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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