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FDA Drug Approval, N018927, TEGRETOL
FDA Drug Approval, N018927, TEGRETOL
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NDA: 018927
Company: NOVARTIS
Drug Name: TEGRETOL
Active Ingredients: CARBAMAZEPINE
Strength: 100MG/5ML
Dosage Form/Route: SUSPENSION;ORAL
Action Date: 12/18/1987
Marketing Status: Prescription
Submission Classification: Type 3 - New Dosage Form
Company: NOVARTIS
Drug Name: TEGRETOL
Active Ingredients: CARBAMAZEPINE
Strength: 100MG/5ML
Dosage Form/Route: SUSPENSION;ORAL
Action Date: 12/18/1987
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
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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