FDA Drug Approval, N016968, MIOSTAT

FDA Drug Approval, N016968, MIOSTAT

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NDA: 016968
Company: ALCON
Drug Name: MIOSTAT
Active Ingredients: CARBACHOL
Strength: 0.01%
Dosage Form/Route: SOLUTION;INTRAOCULAR
Action Date: 09/28/1972
Marketing Status: Prescription
Submission Classification: Type 1 - New Molecular Entity
  • 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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