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FDA Drug Approval, N020385, NICOTROL
FDA Drug Approval, N020385, NICOTROL
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NDA: 020385
Company: PFIZER INC
Drug Name: NICOTROL
Active Ingredients: NICOTINE
Strength: 0.5MG/SPRAY
Dosage Form/Route: SPRAY, METERED;NASAL
Action Date: 03/22/1996
Marketing Status: Prescription
Submission Classification: Type 3 - New Dosage Form
Company: PFIZER INC
Drug Name: NICOTROL
Active Ingredients: NICOTINE
Strength: 0.5MG/SPRAY
Dosage Form/Route: SPRAY, METERED;NASAL
Action Date: 03/22/1996
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
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