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
  • 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. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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