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FDA Drug Approval, N020254, VOLTAREN-XR
FDA Drug Approval, N020254, VOLTAREN-XR
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NDA: 020254
Company: NOVARTIS
Drug Name: VOLTAREN-XR
Active Ingredients: DICLOFENAC SODIUM
Strength: 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: TABLET, EXTENDED RELEASE;ORAL
Action Date: 03/08/1996
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
Company: NOVARTIS
Drug Name: VOLTAREN-XR
Active Ingredients: DICLOFENAC SODIUM
Strength: 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: TABLET, EXTENDED RELEASE;ORAL
Action Date: 03/08/1996
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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