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FDA Drug Approval, N19927, NIZORAL
FDA Drug Approval, N19927, NIZORAL
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NDA: 19927
Company: JANSSEN PHARMS
Drug Name: NIZORAL
Active Ingredients: KETOCONAZOLE
Strength: 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: SHAMPOO;TOPICAL
Action Date: 01/00/1900
Marketing Status: Discontinued
Submission Classification:
Company: JANSSEN PHARMS
Drug Name: NIZORAL
Active Ingredients: KETOCONAZOLE
Strength: 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: SHAMPOO;TOPICAL
Action Date: 01/00/1900
Marketing Status: Discontinued
Submission Classification:
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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