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FDA Drug Approval, N020037, VOLTAREN
FDA Drug Approval, N020037, VOLTAREN
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NDA: 020037
Company: NOVARTIS
Drug Name: VOLTAREN
Active Ingredients: DICLOFENAC SODIUM
Strength: SOLUTION/DROPS;OPHTHALMIC
Dosage Form/Route: Discontinued
Action Date: ORIG-1
Marketing Status: None
Submission Classification: PRIORITY
Company: NOVARTIS
Drug Name: VOLTAREN
Active Ingredients: DICLOFENAC SODIUM
Strength: SOLUTION/DROPS;OPHTHALMIC
Dosage Form/Route: Discontinued
Action Date: ORIG-1
Marketing Status: None
Submission Classification: PRIORITY
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- 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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