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FDA Drug Approval, N050444, MINOCIN
FDA Drug Approval, N050444, MINOCIN
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NDA: 050444
Company: REMPEX
Drug Name: MINOCIN
Active Ingredients: MINOCYCLINE HYDROCHLORIDE
Strength: INJECTABLE;INJECTION
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: None
Submission Classification: UNKNOWN; Orphan
Company: REMPEX
Drug Name: MINOCIN
Active Ingredients: MINOCYCLINE HYDROCHLORIDE
Strength: INJECTABLE;INJECTION
Dosage Form/Route: Prescription
Action Date: ORIG-1
Marketing Status: None
Submission Classification: UNKNOWN; Orphan
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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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