FDA ANDA 216937, Approval Letter for Nimodipine Oral Solution

FDA ANDA 216937, Approval Letter for Nimodipine Oral Solution

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Contents: ANDA approval letter for ANDA 216937, Nimodipine Oral Solution, 3 mg/ml held by Annora Pharma which was approved July 9, 2024.

Drug Name: NIMODIPINE
Active Ingredients: NIMODIPINE
Strength: 3MG/ML
Dosage Form / Route: SOLUTION;ORAL
Action Date: 07/09/2024
Marketing Status: Prescription

  • 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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