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FDA Drug Approval, N022122, VOLTAREN ARTHRITIS PAIN
FDA Drug Approval, N022122, VOLTAREN ARTHRITIS PAIN
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NDA: 022122
Company: HALEON US HOLDINGS
Drug Name: VOLTAREN ARTHRITIS PAIN
Active Ingredients: DICLOFENAC SODIUM
Strength: 1%
Dosage Form/Route: GEL;TOPICAL
Action Date: 10/17/2007
Marketing Status: Over-the-counter
Submission Classification: Type 3 - New Dosage Form
Company: HALEON US HOLDINGS
Drug Name: VOLTAREN ARTHRITIS PAIN
Active Ingredients: DICLOFENAC SODIUM
Strength: 1%
Dosage Form/Route: GEL;TOPICAL
Action Date: 10/17/2007
Marketing Status: Over-the-counter
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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